Trabajos director of investigations en Linden, New JerseyCrear alertas

Job Description General Description: This full-time non-exempt position will supervise well-trained, competent staff of Monitors, who will perform all duties related to safety, security, control of residents and the sanitation of the facility, in accordance with Company and contract requirements. JOB REQUIREMENTS (PERFORMS OTHER WORK-RELATED DUTIES AS ASSIGNED BY IMMEDIATE SUPERVISOR) • Supervise, train, develop and monitor the performance of competent monitors., • Assist in developing and implementing work schedules to cover each shift in the respective facility in, • accordance with contractual requirements., • Ensure that resident supervisors complete all the duties required for each shift in accordance with contract and company requirements, for example: resident formal counts are conducted, • Ensure compliance with all contracts mandated accountability issues included in the duties of resident, • supervisors., • Train new employees, listen and resolve complaints/problems, take corrective or disciplinary action, develop work schedules, monitor post assignments, and approve/deny PTO requests., • Conduct investigations regarding resident misconduct., • Ensure proper contract agency and Company policy orientation/training for operations monitors on a continuing basis., • Effectively communicate to staff, inmates, and visitors in situations requiring tact, diplomacy, understanding, fairness, firmness and good judgment., • Conduct inspections of all housing units and general use areas to ensure that proper standards, facility operating procedures and agency guidelines of security, health and safety sanitation are maintained; direct staff and residents on how to correct problems detected., • Review reports and documentation produced on the shift and ensure to properly process all reports and documents in a timely manner. Prepares disciplinary reports and other administrative reports using appropriate grammar, format, policy and procedures., • Ensures appropriate action is taken to prevent or diffuse potentially disruptive situations., • Ensures there is adequate staffing in post areas led fills in as needed during periods of short staffing., • Ensure that all monitors maintain active CPR and First Aid certifications., • Participate in required training and development sessions., • Maintain a working knowledge of supervisory skills; and participate in the evaluation of operations monitors., • Perform other duties as assigned by the Director of Operations/Sr. Operations Manager. QUALIFICATIONS/SKILL REQUIREMENTS One (1) year as an Operations Monitor or two (2) years related experience in a similar field. Demonstrated leadership experience is preferred. First Aid and CPR certifications, a valid driving license and a clean driving record are required. KNOWLEDGE: Modern correctional principles and practices as they relate to resident accountability; Contracting agency Statement of Work; Company and contracting agency policies and procedures; Company and contracting agency chain of authority; Duties and responsibilities of effective supervisors; Duties and responsibilities of operation monitors. ABILITIES: Work a rotating schedule; Establish authority and communicate for understanding; Communicate effectively, orally and in writing with all levels; and Practice teamwork and manage conflict. Conduct investigations and submit detailed written reports. Identify and report problem areas timely and accurately. Assign and follow-up on assignments for completion. Organize and supervise resources and projects; Train, evaluate, review, develop, discipline, and document personnel actions. Establish and maintain effective working relationships with staff and co-workers; Meet contracting agency clearance requirements. EDUCATION REQUIREMENTS High School Diploma (or equivalent) required. An associate’s degree preferred with advanced supervisory/management training.

Job Title: Quality Specialist – II Duration: 24 Months Location: Rahway, NJ 07065 Hybrid(3 days onsite flexible) Pay Rate: $45/hr. on W2 Work Arrangement: Hybrid Employment Type: Contract Domain: Pharmaceutical Application Deadline: November 13th, 2026 Description: Education Minimum Requirement • Bachelor degree, technical emphasis in an appropriate scientific or engineering field preferred; Required Experience and Skills • Minimum of 3 to 6 years of relevant post-degree experience in the Pharmaceutical or equivalent industry (Good Manufacturing Practice (GMP) related field) including Technical, Engineering, Quality or Operations., • Ability to follow established procedures, work instructions, and defined decision criteria., • Strong attention to detail and ability to maintain accurate documentation., • Effective written and verbal communication skills, particularly when obtaining information and following up with internal stakeholders or clinical sites., • Ability to manage assigned activities and meet established timelines., • Ability to recognize issues requiring escalation and seek guidance when appropriate., • Effectiveness and creativity in approaching and solving technical problems., • Basic understanding of the use and maintenance of Microsoft applications (such as MS Excel, Outlook, and/or MS Access)., • Demonstrated teamwork skills and the ability to work independently., • Willingness and ability to learn complaint-management and clinical-supply systems and processes. Preferred Experience and Skills • Previous experience in clinical supply, distribution, logistics, customer service, complaint intake, or quality-related operations., • Previous experience in quality control, quality assurance, auditing or regulatory affairs., • Ability to independently manage multiple priorities., • Familiarity with clinical trials or the clinical supply chain., • Experience with systems such as Veeva, SAP, TrackWise, or other quality/supply-chain systems is preferred but not required. Responsibilities This position reports to the Associate Director, Global Clinical Complaints, Global Development Quality, and supports the clinical complaint process for clinical supplies used in worldwide clinical trials. • The primary focus of this role is the intake, processing, documentation, coordination, and follow-up of distribution-related clinical complaints, including issues associated with shipment, delivery, transportation and handling of clinical supplies, • The individual will communicate with clinical sites and internal stakeholders to obtain required information, ensure complaints are accurately documented and routed to the appropriate investigating function, and monitor activities through completion. Primary Responsibilities • Receive and process distribution-related clinical complaints in accordance with established procedures and work instructions., • Communicate with clinical sites and internal stakeholders to obtain required complaint information and supporting documentation to ensure they meet establish criteria for processing, • Review complaint information for completeness and perform initial categorization using established criteria and decision tools., • Enter, maintain, and update complaint information within applicable complaint management systems., • Route complaints to the appropriate functional area for investigation and follow up in accordance with established procedures and to support timely completion and on-time closure of reported distribution complaint., • Support coordination of clinical supply activities associated with distribution-related complaints, including usability assessment of supplies impacted by temperature excursions during shipping, shipment issues/errors, shipments to incorrect destinations, temperature device malfunctions, etc. Key Points • Role: Two-year contingent assignment supporting client’s Clinical Complaints Team, primarily handling distribution-related complaints., • Responsibilities: Investigate temperature excursions, shipping errors, incorrect destinations, and temperature-device malfunctions; coordinate investigations, identify root causes, and support corrective actions., • Schedule: Three days onsite and two remote. Wednesday is preferred, not mandatory. No travel., • Collaboration: Work with the complaints team, clinical sites, West Point, Switzerland, and external partners such as Almac and Fisher. Key Skills • Investigation and analytical thinking: Gather evidence, connect findings, and draw supported conclusions., • Attention to detail: Maintain accurate complaint records and meet closure timelines., • Root-cause analysis and corrective actions., • Communication and follow-through: Coordinate with internal sites and external suppliers through investigation completion., • Teamwork, flexibility, and adaptability within a clinical environment., • Complaint-system proficiency: Experience with the database transcribed as “Veeva” is beneficial, but training is available; confirm the product name. Key Experience • Product quality complaint experience is strongly preferred, even though the assignment focuses on distribution complaints—the processes use the same SOP., • Pharmaceutical industry experience, preferably in clinical supplies or the clinical environment., • Relevant exposure to distribution issues, temperature excursions, shipping investigations, and complaint handling., • Commercial pharmaceutical experience remains acceptable; clinical experience is a preference, not a deal breaker. BENEFITS Medical | Dental | Vision | 401(k) EEOC Compliance: We are an equal opportunity employer, and all qualified applicants will receive consideration for employment. DISCLAIMER AI Usage Policy: Pacer Group uses AI to assist in screening applications. Final hiring decisions are made by human recruiters based on qualifications and experience.

McCarter & English LLP is seeking an Information Security Engineer who will be based in our Newark, NJ office. The salary for this hybrid position is $120,00 to $150,000 annually. If you have the appropriate experience, we invite you to consider joining our team. Candidates who receive an offer of employment will be processed through a background check which will be an individualized assessment based on the applicant’s or employee’s specific record and the duties and requirements of the specific job. Please send your resume and cover letter to the attention of Christine Lydon, Esq., at recruiting@mccarter.com. Reports to: Director of Information Security, Data Privacy & Information Governance Schedule: Staggered work schedule, generally 12:00 PM to 8:00 PM ET, with flexibility based on operational needs. The Information Security Engineer is responsible for maintaining and supporting the firm's cybersecurity tools, systems, and operations. This hands-on technical role ensures alignment with established policies, procedures, and security objectives by assisting in the implementation, configuration, and monitoring of security technologies. The Information Security Engineer will work closely with IT and security teams to identify and respond to threats, remediate vulnerabilities, and uphold the security of firm assets and data. This position will also have a strong focus on proactive threat intelligence research, threat hunting, and security investigations, including identifying emerging threats, evaluating potential exposure to the firm and its clients, and recommending appropriate defensive actions. Responsibilities • Monitor and support daily security operations, including the analysis, maintenance, and optimization of cybersecurity tools and infrastructure., • Investigate, respond to, and document security incidents, including root cause analysis, corrective actions, and recommendations to improve security controls., • Conduct proactive threat intelligence research on emerging threats, threat actors, and tactics, techniques, and procedures (TTPs) relevant to the firm and the legal industry., • Perform threat hunting and analyze security telemetry across endpoint, network, identity, email, and cloud platforms to identify suspicious activity, indicators of compromise, and potential security exposures., • Manage and contribute to cybersecurity projects, including security tool deployments, configuration enhancements, and remediation efforts., • Support the firm's vulnerability management program, including identifying, prioritizing, and coordinating remediation of security vulnerabilities., • Maintain and enhance security technologies, including SIEM, EDR, firewalls, identity protection, vulnerability management, and email security platforms., • Collaborate with IT teams to implement security best practices, strengthen technical controls, and address identified security risks., • Support security assessments, client security questionnaires, compliance initiatives, and audit-related remediation efforts., • Contribute to security awareness initiatives in partnership with the Information Governance team., • Coordinate with external security providers and incident response partners on investigations, escalations, and security initiatives., • Develop and maintain security documentation, policies, procedures, and operational runbooks to improve security operations and incident response capabilities., • Provide extended operational coverage through a staggered work schedule to support security monitoring, investigations, and incident response beyond traditional business hours. Experience and Requirements • Bachelor's degree in information systems, cybersecurity, or a related field, or equivalent experience., • Minimum of 4 years of experience in information security, security engineering, security operations, or a related IT security role., • CISSP or similar certification required; additional certifications such as CISM, GCIH, GCIA, GCFA, or other GIAC certifications are a plus., • Hands-on experience with security technologies, including SIEM, EDR, vulnerability management, firewalls, identity protection, and email security platforms., • Demonstrated experience investigating security incidents, analyzing security events, and recommending appropriate response and remediation actions., • Experience with threat intelligence research, threat hunting, and open-source intelligence (OSINT) techniques., • Familiarity with MITRE ATT&CK, threat actor tactics, techniques, and procedures (TTPs), and common attack methodologies., • Understanding of information security frameworks such as NIST CSF or ISO 27001, as well as relevant regulatory and compliance requirements., • Strong analytical, troubleshooting, and problem-solving skills, with the ability to work independently and manage multiple priorities., • Effective written and verbal communication skills, including the ability to document investigations, communicate findings, and provide recommendations., • Ability to collaborate effectively with internal teams and external security partners., • Willingness to work a staggered schedule to provide extended security operations coverage through evening hours. Note: While the list of essential duties is intended to be as inclusive as possible, there may be other duties, which are essential to particular positions within the class. Benefits (if FTE requirements met): • Firm-Paid: Basic life and accidental death and dismemberment (AD&D) insurance and short-term (ST) and long-term (LT) disability benefits., • Health & Wellness: Comprehensive medical/prescription drug coverage (the Firm pays a share of the cost), including a high deductible health plan with an annual Firm health savings account (HSA) contribution., • Employee-Paid Voluntary Benefits: Dental and vision coverage, supplemental health plans (accident, cancer and critical illness), flexible spending accounts, optional life and AD&D insurance (supplemental employee, spouse and child) and supplemental STD coverage., • Retirement: 401(k) plan offering three types of contributions: pre-tax, Roth and after-tax contributions., • Time Off: Paid Time Off (PTO), paid holidays, and leaves of absence to support work-life balance (e.g. parental leave) Additional Benefits: • Free and confidential employee assistance program (EAP) and behavioral health services program, • Firm-paid back-up child/elder care, academic support and pet care program, • Tax-advantaged college savings 529 Plan, • Employee discounts through Working Advantage Other Compensation: • Eligibility for discretionary bonus. McCarter & English, LLP is an Equal Opportunity Employer

The Director, Employee Relations & Workforce Practices will lead the development of a modern, data-informed approach to employee relations, workforce-risk management, investigations, and workplace practices. Leads the enterprise Employee Relations & Workforce Practices function and is accountable fo

Job Title: Quality Specialist – II \n Duration: 24 Months \n Location: Rahway, NJ 07065 Hybrid(3 days onsite flexible) \n Pay Rate: $45/hr. on W2 \n Work Arrangement: Hybrid \n Employment Type: Contract \n Domain: Pharmaceutical \n Application Deadline: November 13th, 2026 \n \n Description: \n \n Education Minimum Requirement \n • Bachelor degree, technical emphasis in an appropriate scientific or engineering field preferred; \n \n Required Experience and Skills \n • Minimum of 3 to 6 years of relevant post-degree experience in the Pharmaceutical or equivalent industry (Good Manufacturing Practice (GMP) related field) including Technical, Engineering, Quality or Operations. \n • Ability to follow established procedures, work instructions, and defined decision criteria. \n • Strong attention to detail and ability to maintain accurate documentation. \n • Effective written and verbal communication skills, particularly when obtaining information and following up with internal stakeholders or clinical sites. \n • Ability to manage assigned activities and meet established timelines. \n • Ability to recognize issues requiring escalation and seek guidance when appropriate. \n • Effectiveness and creativity in approaching and solving technical problems. \n • Basic understanding of the use and maintenance of Microsoft applications (such as MS Excel, Outlook, and/or MS Access). \n • Demonstrated teamwork skills and the ability to work independently. \n • Willingness and ability to learn complaint-management and clinical-supply systems and processes. \n Preferred Experience and Skills \n • Previous experience in clinical supply, distribution, logistics, customer service, complaint intake, or quality-related operations. \n • Previous experience in quality control, quality assurance, auditing or regulatory affairs. \n • Ability to independently manage multiple priorities. \n • Familiarity with clinical trials or the clinical supply chain. \n • Experience with systems such as Veeva, SAP, TrackWise, or other quality/supply-chain systems is preferred but not required. \n \n Responsibilities \n This position reports to the Associate Director, Global Clinical Complaints, Global Development Quality, and supports the clinical complaint process for clinical supplies used in worldwide clinical trials. \n • The primary focus of this role is the intake, processing, documentation, coordination, and follow-up of distribution-related clinical complaints, including issues associated with shipment, delivery, transportation and handling of clinical supplies \n • The individual will communicate with clinical sites and internal stakeholders to obtain required information, ensure complaints are accurately documented and routed to the appropriate investigating function, and monitor activities through completion. \n \n Primary Responsibilities \n • Receive and process distribution-related clinical complaints in accordance with established procedures and work instructions. \n • Communicate with clinical sites and internal stakeholders to obtain required complaint information and supporting documentation to ensure they meet establish criteria for processing \n • Review complaint information for completeness and perform initial categorization using established criteria and decision tools. \n • Enter, maintain, and update complaint information within applicable complaint management systems. \n • Route complaints to the appropriate functional area for investigation and follow up in accordance with established procedures and to support timely completion and on-time closure of reported distribution complaint. \n • Support coordination of clinical supply activities associated with distribution-related complaints, including usability assessment of supplies impacted by temperature excursions during shipping, shipment issues/errors, shipments to incorrect destinations, temperature device malfunctions, etc. \n Key Points \n • Role: Two-year contingent assignment supporting client’s Clinical Complaints Team, primarily handling distribution-related complaints. \n • Responsibilities: Investigate temperature excursions, shipping errors, incorrect destinations, and temperature-device malfunctions; coordinate investigations, identify root causes, and support corrective actions. \n • Schedule: Three days onsite and two remote. Wednesday is preferred, not mandatory. No travel. \n • Collaboration: Work with the complaints team, clinical sites, West Point, Switzerland, and external partners such as Almac and Fisher. \n \n Key Skills \n • Investigation and analytical thinking: Gather evidence, connect findings, and draw supported conclusions. \n • Attention to detail: Maintain accurate complaint records and meet closure timelines. \n • Root-cause analysis and corrective actions. \n • Communication and follow-through: Coordinate with internal sites and external suppliers through investigation completion. \n • Teamwork, flexibility, and adaptability within a clinical environment. \n • Complaint-system proficiency: Experience with the database transcribed as “Veeva” is beneficial, but training is available; confirm the product name. \n \n Key Experience \n • Product quality complaint experience is strongly preferred, even though the assignment focuses on distribution complaints—the processes use the same SOP. \n • Pharmaceutical industry experience, preferably in clinical supplies or the clinical environment. \n • Relevant exposure to distribution issues, temperature excursions, shipping investigations, and complaint handling. \n • Commercial pharmaceutical experience remains acceptable; clinical experience is a preference, not a deal breaker. \n \n BENEFITS \n Medical | Dental | Vision | 401(k) \n \n EEOC Compliance: \n We are an equal opportunity employer, and all qualified applicants will receive consideration for employment. \n \n DISCLAIMER \n AI Usage Policy: Pacer Group uses AI to assist in screening applications. Final hiring decisions are made by human recruiters based on qualifications and experience. \n

Job Description Director of Quality | Dietary Supplement Manufacturing About the Role We're partnering with a growing supplement manufacturer that is looking for a Director of Quality to own its quality and compliance function. You'll set the strategy and stay close to daily execution, making sure every product that ships is safe, consistent, and fully compliant. You'll work closely with production, R&D, regulatory, procurement, and customers, and you'll be the face of quality during regulatory inspections and customer audits. This is an in-person position just outside of New Jersey What You'll Do • Build, maintain, and continuously strengthen the quality management system, ensuring alignment with FDA dietary supplement cGMP regulations (21 CFR Part 111), • Establish and enforce SOPs and quality policies across the organization, and train teams on quality expectations, • Own the supplier quality program, including approval of new vendors, on-site and remote audits, and ongoing performance monitoring, • Lead internal audit activity and keep the facility inspection-ready at all times, • Act as the lead quality contact for FDA inspections, third-party audits, and customer visits, • Approve incoming material documentation before use in production and release finished-product documentation to customers, • Review and sign off on analytical methods, test data, and specifications across raw, in-process, and finished materials, • Manage the stability and shelf-life program, • Lead investigations into deviations, out-of-specification results, and customer complaints, and drive corrective and preventive actions, • Run the retain sample program, including sensory evaluation of production lots, • Support customer-driven certification and qualification projects, • Partner with R&D, production, and regulatory teams so quality is built in from development through manufacturing, • Track and trend key quality metrics, such as complaints, deviations, and audit findings, to drive ongoing improvement What You Bring • Working knowledge of FDA regulations and cGMP, including 21 CFR Part 111, and sound quality system principles, • Hands-on experience with supplier qualification, auditing, and compliance, • Leadership presence and the ability to collaborate across departments, • Strong written communication, documentation, and problem-solving skills, • Comfort with Microsoft Office; experience with SharePoint or similar document-sharing platforms is a plus; ERP familiarity is helpful Background • Bachelor's degree in a scientific field such as chemistry, microbiology, or food science (or equivalent), • 5 to 10 years in quality management in the dietary supplement or nutraceutical industry, including exposure to laboratory operations Compensation: $140,000 - $165,000 If this sounds like the position you have been waiting for, please apply using the online application or the link below. All inquiries are strictly confidential. Our focus is to assist you in making your best next career move, and we will not use your information for any other purpose. Kalon Search is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. www.KalonSearch.com

Job Description Who we are at Osmo: Osmo is a digital olfaction company, on a mission to give computers a sense of smell to improve the health and wellbeing of human life. Why? Our sense of smell both enriches and saves lives, and has a deep and direct connection to our emotions and memory. Olfactory Intelligence has applications across industries including fragrance, manufacturing, security, medicine, and more. We believe in the power of automation and thoughtfully applied AI/ML to solve problems beyond the reach of human intuition alone. We're headquartered in Elizabeth, NJ, with an additional office in Somerville, MA. We provide complimentary shuttle service from Brooklyn and Newark, NJ. About the Role This is a ground-floor opportunity to build and lead Quality Control at Osmo. You'll own quality on both ends of the plant, raw materials coming in and finished fragrance going out, using real fragrance-industry judgment that automated testing alone can't provide. You'll have the autonomy to build the program end to end and the trust to make real-time calls from day one. What You'll Do Own Raw Material Quality — Judge incoming material results from automated testing, deciding when an out-of-spec reading is a real defect versus normal variation in a natural material. Apply Trained Olfactive Judgment — Evaluate raw materials and finished goods using olfactive evaluation the equipment can't replicate. Protect Finished Goods Quality — Run triangulation testing on outgoing product to confirm it matches prior batches before it reaches a customer. Build the QC Program — Design and continuously improve the process, documentation, and systems this function runs on, picking up from groundwork already laid. Make the Call — Decide accept or reject in real time, multiple times a day, escalating only genuinely ambiguous cases. Fix What's Broken — Spot gaps in the current process and drive the fix, rather than operating inside a system someone else already defined. Own Investigations — Lead root cause analysis on non-conforming materials, out-of-spec results, and customer quality concerns, and drive corrective actions. Run the Lab — Maintain lab documentation, SOPs, method records, and equipment calibration and qualification. Track Quality KPIs — Monitor and report on QC turnaround time, effectiveness, and recurring issues. Build the Team — Grow and lead a QC team as headcount is added. Partner Across the Floor — Work directly with Purchasing, Warehouse, Shipping and Receiving, Fragrance Development, Production, and the internal AI team on raw material and finished goods decisions. Who You Are 5+ Years in Fragrance QC — Direct fragrance industry experience required; adjacent industries like flavor, cosmetics, or specialty chemicals don't clear the bar here. 8 to 12 years is ideal. A Builder, Not Just an Operator — You've stood up or fixed a QC process before, not only executed inside one someone else built. Trained Nose — Organoleptic and sensory evaluation skill specific to fragrance raw materials and finished goods. Independent Decision-Maker — Comfortable making high-frequency accept or reject calls without over-escalating routine judgment. Quality Systems Fluent — Working knowledge of quality documentation, audits, and CAPA/root cause processes in a regulated manufacturing environment. Direct Communicator — Low-bureaucracy, thrives in a fast-moving, still-being-built environment. Technical Degree Preferred — Bachelor's in Chemistry, Chemical Engineering, or a related scientific field preferred; equivalent hands-on experience accepted in place of a degree. On Site in Elizabeth, NJ — In the plant 5 days a week. What Success Looks Like (First 6-12 Months) Establish a real, working quality QC program from a process and systems standpoint, building on the groundwork already started. Qualify raw materials at scale. Get product to customers cleanly and consistently, without holds or rejections after the fact. What We Offer (Full Time Roles Only) Ground-Floor Ownership — Build a quality function from the foundation up, not maintain someone else's finished system. Real Growth Path — Room to grow into a Director of QC role as Osmo scales to multiple sites, with potential to grow the function into a broader quality department. Catered Lunch — Mon/Wed/Fri; NJ and Brooklyn shuttles 401(k) savings plan and employer match Competitive salary and meaningful equity in a high-growth company Flexible PTO and paid family leave Commuter benefits (pre-tax transit and parking) If this role inspires you we’d encourage you to apply. We are committed to recruiting, developing, and retaining an incredible team optimized for a diversity of thought, background, and approaches. For all Full-Time Employees, compensation is just one component of Osmo’s total rewards approach, which is designed to support the well-being, growth, and long-term success of our team members. Depending on the role, this may include base salary or contract-based pay, along with access to health, dental, and vision coverage; a 401(k) retirement savings plan with company match; flexible paid time off and company holidays; and equity or incentive compensation for eligible roles. Actual compensation will vary based on factors such as experience, skills, location, internal equity, and other relevant business considerations. Osmo regularly reviews pay ranges and compensation structures to ensure they remain competitive, equitable, and aligned with current market data. All employment decisions and responsibilities are determined based on current ability and your ability to grow, without regard to race, color, gender identity, sex, sexual orientation, religion, age, marital status, physical, mental, or sensory disability, or any other characteristic protected by applicable law. Recruitment & Staffing Agencies: Osmo does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Osmo or its employees is strictly prohibited unless contacted directly by the Osmo Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Osmo and Osmo will not owe any referral or other fees with respect thereto. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire Compensation Range: $105K - $140K

Job Description Job Title: People & Culture Manager Company: StriveWell Location: New Jersey (Hybrid) Employment Type: Full-Time Reports To: CEO Travel: Local travel between company locations may be required. Compensation: $70,000–$74,000 annually Benefits: Specific benefits will be discussed during the hiring process. Job Summary StriveWell is seeking a highly organized, dependable, and people-focused People & Culture Manager to oversee day-to-day human resources and people operations across its growing portfolio of health and wellness brands, including StriveWell, SWTHZ, and STRONG Pilates. Reporting directly to the CEO, this role is responsible for managing the full employee lifecycle, including payroll processing, HRIS administration, onboarding, offboarding, employee relations, performance management, compliance, and employee engagement. The ideal candidate has 3–5 years of progressive HR or People Operations experience, with strong hands-on payroll processing skills and the ability to independently manage essential HR functions across multiple locations. This position requires someone who is detail-oriented, approachable, organized, and comfortable taking ownership of recurring HR processes while collaborating with leadership and external advisors on complex employee relations, legal matters, and strategic People decisions. Essential Duties and Responsibilities • Manage daily HR and People Operations across StriveWell, SWTHZ, and STRONG Pilates locations., • Serve as the primary point of contact for employee and manager questions regarding HR policies, payroll, benefits, and workplace concerns., • Independently manage the full payroll process, including preparation, processing, submission, and post-payroll review across multiple entities and locations., • Review and verify employee timecards, salaries, commissions, bonuses, PTO, deductions, reimbursements, and other payroll-related information., • Process payroll adjustments related to new hires, terminations, promotions, compensation changes, transfers, and employee deductions., • Review payroll reports, identify discrepancies, coordinate corrections, and process off-cycle payments when necessary., • Maintain payroll schedules and ensure managers submit and approve timekeeping records within established deadlines., • Coordinate with payroll providers and Finance to ensure accurate payroll reporting, reconciliation, and compliance., • Administer and maintain the company's Human Resources Information System (HRIS), ensuring accurate employee information and records., • Manage the onboarding process, including employment documentation, background checks, I-9 verification, orientation, HRIS setup, and payroll enrollment., • Coordinate employee offboarding, including final payroll, benefits, documentation, system access, and personnel records., • Develop and maintain HR policies, standard operating procedures (SOPs), templates, checklists, and employee documentation., • Provide guidance to managers on employee attendance, performance expectations, workplace policies, coaching, and accountability., • Support performance management processes, including employee evaluations, performance documentation, and Performance Improvement Plans (PIPs)., • Address routine employee relations concerns while escalating complex investigations, legal matters, terminations, and high-risk situations to the CEO and external advisors., • Coordinate employee engagement activities, recognition programs, internal communications, and workplace culture initiatives., • Support compliance with applicable federal, state, and local employment laws and regulations., • Assist with benefits administration and maintain relationships with external HR, payroll, and benefits providers., • Track and report HR metrics, including employee headcount, turnover, retention, hiring, payroll, and performance data., • Collaborate with the Director of Operations, Finance Operations Manager, and other department leaders to improve People Operations., • Identify opportunities to streamline, standardize, and automate HR processes across company locations., • Maintain confidentiality when handling employee information, payroll records, and sensitive workplace matters.Required Qualifications, • 3–5 years of progressive experience in Human Resources, People Operations, payroll administration, or an HR Generalist role., • Demonstrated hands-on experience independently preparing, processing, reviewing, and administering payroll., • Strong knowledge of payroll procedures, timekeeping systems, employee documentation, and HR operations., • Experience administering HRIS platforms and maintaining accurate employee records., • Experience managing employee onboarding, offboarding, employee relations, and performance management processes., • Working knowledge of federal, state, and local employment regulations and HR compliance requirements., • Strong organizational skills with excellent attention to detail and accuracy., • Ability to independently manage multiple responsibilities, prioritize deadlines, and maintain consistent follow-through., • Excellent verbal and written communication skills., • Strong interpersonal skills with the ability to support employees, managers, and executive leadership., • Ability to handle confidential and sensitive employee information with professionalism and discretion., • Strong problem-solving skills and sound judgment when addressing workplace concerns., • Ability to work collaboratively with cross-functional teams and external service providers., • Proficiency with Microsoft Office, Google Workspace, HRIS platforms, and payroll systems.Preferred Qualifications, • Experience processing payroll across multiple business entities or locations., • Previous HR experience supporting multi-location or multi-brand organizations., • Experience working in fitness, wellness, hospitality, retail, or franchise environments., • Experience implementing or improving HR policies, workflows, and standard operating procedures., • Familiarity with employee engagement programs, performance management systems, and HR reporting., • Experience coordinating employee benefits administration and working with external payroll or HR providers., • Experience supporting organizational growth and improving HR processes., • SHRM-CP, PHR, or similar professional HR certification., • Experience working directly with executive leadership or business owners.Work Environment / Schedule, • Full-time position based in New Jersey with a hybrid work arrangement., • Supports multiple health and wellness brands, including StriveWell, SWTHZ, and STRONG Pilates., • Reports directly to the CEO and collaborates with department leaders across company locations., • May require occasional travel between business locations for meetings, employee support, or operational needs., • Must be available during regular business hours to address employee concerns, payroll deadlines, and HR-related matters., • Requires the ability to manage multiple priorities and recurring deadlines in a growing, fast-paced organization., • Work involves regular use of HRIS platforms, payroll software, spreadsheets, and other administrative systems., • Must maintain confidentiality and professionalism when handling sensitive employee and company information.Compensation and Benefits, • Annual salary of $70,000–$74,000, depending on experience and qualifications., • Hybrid work arrangement offering flexibility between remote and on-site responsibilities., • Opportunity to work directly with the CEO and senior leadership., • Exposure to multiple growing brands within the health and wellness industry., • Opportunity to take ownership of People Operations and contribute to organizational growth., • Professional development opportunities in HR operations, payroll management, employee relations, and leadership., • Specific employee benefits and additional compensation details will be discussed during the hiring process.EEO Statement, • We are an Equal Opportunity Employer and consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other legally protected characteristic under applicable federal, state, or local law.

Job DescriptionCompliance Auditor Remote Position Ascend Hospice | Administration Reports to: National Director of Compliance Ascend Hospice is seeking a Compliance Auditor to support our Corporate Compliance Program. In this role, you will conduct independent audits of hospice operations, review clinical and billing documentation, support responses to payer audits, and help leaders address compliance risks. What you’ll do Audit hospice operations, clinical documentation, and billing practices for compliance with Medicare requirements, accreditation standards, and company policies. Coordinate responses to Additional Documentation Requests (ADRs) and other payer or government audits. Review records for completeness, track audit deadlines and outcomes, and escalate documentation gaps. Analyze findings and denial trends, identify root causes, and prepare reports for leadership. Track corrective action plans and conduct follow-up audits to confirm improvements are effective. Monitor regulatory changes, support policy updates, and assist with compliance investigations and QAPI activities. Qualifications A current RN license to practice in at least one state served by Ascend Hospice is preferred. Candidates without an RN license must hold at least one of these certifications: CHC, CHCA, RHIA, RHIT, CPC, or CCS. Experience in healthcare compliance, auditing, hospice operations, Medicare reviews, ADR management, medical record review, reimbursement, or regulatory oversight. Strong analytical, organizational, communication, and report writing skills. Ability to manage multiple priorities and deadlines independently. Proficiency with Microsoft Excel, Word, and Outlook. A bachelor’s degree in a related field and three years of related healthcare experience are preferred. Hospice, home health, or post-acute experience is strongly preferred. Familiarity with Medicare hospice regulations, government audits, QAPI, or CHAP accreditation is a plus. This position involves extensive computer and medical record review, with periodic travel to agency locations as needed. Ascend Hospice is an equal opportunity employer.

Job Description $5000.00 Sign on bonus!!! and Daily Pay!!! Required Qualifications A Nursing Degree from an accredited college or university or a graduate of an approved LPN/LVN program. Prior experience in long-term care preferred but not required. Current unrestricted license as a Registered Nurse (RN) or Licensed Practical Nurse (LPN) in practicing state. Current CPR certification. Major Duties and Responsibilities Directs the daily activities of the certified nursing assistants in accordance with current federal, state and local regulations and guidelines and established facility policies and procedures. Ensures that policies and procedures are complied with by nursing personnel assigned. Participates in the admission, discharge and transfers of residents as required. Observes for changes in residents’ status, notifying the physician and resident’s family or representative and documenting accordingly. Transcribes physician orders to medical record and carries out orders as written. Prepares and administers medications as per physicians’ orders and observes for adverse effects. Performs wound treatments as per physicians’ orders, observes for changes and documents accordingly. Schedules follow up appointments for residents and transportation needs as indicated. Provides nursing leadership to nursing personnel assigned to the unit. Provides direct care skills such as colostomy changes, tube feedings, wound care, suctioning, IV administration, etc. in accordance with current policies and procedures. Performs rounds to ensure resident needs are being met and personnel are performing their assigned duties. Collaborates with other members of the interdisciplinary team as needed to ensure residents’ needs are holistically met. Informs appropriate departments of concerns or complaints and files grievances as necessary. Reports any incidents or unusual occurrences to the supervisor, unit manager, assistant director or nursing or director of nursing and participates in the investigative process as needed. Participates in end of life care as required. Ensures that there is adequate stock of medications, supplies, equipment and notifies appropriate personnel of needs. Initiates, reviews and updates care plans as required. Promotes teamwork, mutual respect, and effective communication. Participates in the survey process when inspection surveys arise. Reports any allegations of abuse, neglect, misappropriation of property, exploitation, or mistreatment of residents to administrator. Protects residents from abuse, and cooperates with all investigations. Reports any occupational exposures to blood, body fluids, infectious materials, and/or hazardous chemicals in accordance with facility policy. Participates in all life safety and emergency drills and trainings. Fulfills responsibilities as assigned during implementation or activation of the facility’s emergency plan.

Job Description A Senior Quality Assurance (QA) Management role in cheese and dairy manufacturing (such as a Director of Quality Assurance or Plant/Corporate QA Manager oversees company-wide food safety, regulatory compliance, and product integrity. Position Overview  Role Title: Director of Quality Assurance / Senior QA Manager (Dairy Cheese Operations)  Industry Focus: Dairy Processing, Cheese Manufacturing, Cultured Products, and Conversion Operations  Reporting To: President, Chief Operating Officer, or VP of Operations / Corporate Quality  Scope: Plant-level; Innovative Food Science, FDA Labeling; Product development with knowledge of current technologies; Shelf-life, HACCP; Food Safety Auditing Key Responsibilities Duties  Strategy Leadership: Direct and mentor QA teams, lab supervisors, across multi-shift cheese production environments. (working in line with mid-level QA team)  Regulatory GFSI Compliance: Maintain and audit programs under FDA/USDA, FSMA, Grade A Pasteurized Milk Ordinance (PMO), HACCP, Preventive Controls (PC), and global standards like SQF or BRC.  Cheese Dairy Technical Oversight: Oversee specialized cheese-making quality metrics—including milk composition, pasteurization/thermal controls, starter culture performance, moisture/pH levels, curing/aging environments, and shelf-life analysis.  Preventive Corrective Action: Lead Root Cause Analysis (RCA), Corrective and Preventive Actions (CAPA), customer complaint investigations, and hold/release protocols for finished cheese and ingredients.  Traceability Crisis Management: Direct mock recalls, rapid ingredient-to-finished-product tracking exercises, and act as a core leader on the Plant Crisis Management / Recall Team.  Cross-Functional Partnership: Collaborate closely with Operations, RD, Procurement, Sales, and Farm-to-Plant milk suppliers to uphold farm-to-table quality standards. Qualifications Requirements  Education: Bachelor’s degree in food science, Dairy Science, Microbiology, or a related technical discipline (Masters or advanced degree strongly preferred).  Experience: Progressive leadership experience (typically 7–10+ years) in dairy or cultured cheese manufacturing, with deep knowledge of processing and conversion lines.  Certifications: HACCP Training, SQF Practitioner, PCQI (Preventive Controls Qualified Individual), and Grade A dairy regulatory familiarity.  Technical Skills: Proficiency in Laboratory Information and food safety auditing.  Computer Skills: Excel, MS Word, Adobe PDF Editing  Communicatin Skills: Proficiency in written communication

Job Description Lantheus (NASDAQ: LNTH) is the leading radiopharmaceutical-focused company, delivering life-changing science to enable clinicians to Find, Fight and Follow disease to deliver better patient outcomes. Headquartered in Massachusetts with offices in New Jersey, Canada, Germany, Sweden, Switzerland and United Kingdom, Lantheus has been providing radiopharmaceutical solutions for nearly 70 years. Today, we’re expanding our portfolio and pipeline across oncology, neurology and cardiology. Through recent acquisitions, along with strategic partnerships across the life sciences ecosystem, we are accelerating our efforts to advance precision medicine and improve patient outcomes around the world. At Lantheus we are purpose-driven, and every employee plays a vital role in our success. We’re dedicated to cultivating a high-growth, forward-thinking culture where innovation thrives and diverse perspectives drive meaningful progress. Join us and be part of a company where your contributions make a real impact, because we know someone’s health is in our hands. Summary of role We are seeking a Process Engineer II who will be responsible for providing technical support for pharmaceutical and radiopharmaceutical manufacturing operations throughout the product lifecycle. This role serves as a subject matter expert for manufacturing processes, supporting technology transfer, process validation, equipment qualification, investigations, process monitoring, and continuous improvement initiatives. The Process Engineer II is responsible for planning, executing, and maintaining validation activities to support pharmaceutical and/or radiopharmaceutical manufacturing operations. This role acts as a study director for assigned process validation activities and ensures manufacturing processes, equipment, utilities, automation systems, cleaning, and sterilization processes remain in a validated state and compliant with applicable regulatory requirements. The Process Engineer II works independently while collaborating closely with Manufacturing, Engineering, Quality, MSAT, and external partners to support project execution, inspection readiness, and continuous improvement of the process validation program. This position is based in Springfield, New Jersey and requires a presence on-site three days per week, and open to applicants authorized to work for any employer within the United States. Responsibilities • Serve as the technical owner for assigned manufacturing processes, providing engineering support throughout the product lifecycle from technology transfer through commercial manufacturing., • Support the design, implementation, qualification, and lifecycle management of manufacturing equipment, utility systems, automation systems, and facility infrastructure used in GMP operations., • Author and review technical documentation including system definitions, user requirements, risk assessments, qualification and validation documentation, engineering studies, investigations, and technical reports. The role would support creation of URS, SIA, risk assessments, design qualifications, verification packages, and performance qualification activities., • Lead and support commissioning, qualification, verification, performance qualification, requalification, and process validation activities using risk-based validation and good engineering practices., • Responsible for execution of process validation activities, including authoring and reviewing validation protocols, coordinating and/or executing protocol execution, and authoring final validation reports., • Provide on-floor technical support during engineering, clinical, process validation, and commercial manufacturing campaigns to ensure safe, compliant, and reliable execution of manufacturing operations., • Provide process validation support for manufacturing processes, equipment, utilities, automation systems, cleaning, and sterilization to support routine operations and facility or process change projects., • Represent the Process Validation function on cross‑functional project teams and provide regular updates on validation status, schedule adherence, and identified risks., • Ensure validation protocols and reports are developed, executed, and approved in compliance with applicable validation guidelines, cGMP requirements, and global regulatory expectations (e.g., FDA, EMA, PIC/S)., • Independently collect, organize, analyze, and evaluate validation data and communicate progress, issues, and risks to validation management., • Participate in project team meetings to ensure validation activities meet established timelines and support business needs., • Support inspection readiness activities, participate in regulatory agency inspections, and provide audit support as required., • Collaborate effectively with Manufacturing, Engineering, Quality, MSAT, contractors, consultants, and vendors to ensure coordinated execution of process validation activities., • Lead continuous improvement initiatives for the process validation program, including revision and creation of validation procedures, templates, and best practices., • Actively promote safety rules and awareness and demonstrate good safety practices at all times., • Actively demonstrate Lantheus values of accountability, quality, efficiency, customer service, collaboration, and safety. Basic Qualifications • Bachelor’s degree in engineering, Life Sciences, or a related scientific discipline., • Minimum of 3+ years of process and/or equipment validation experience in the pharmaceutical, biopharmaceutical, or medical device industry., • Demonstrated hands‑on validation experience with pharmaceutical manufacturing processes and systems including radiopharmaceutical dispensing systems and radiopharmaceutical synthsizers., • Demonstrated knowledge of cGMP requirements, pharmaceutical process validation practices, and change control processes., • Proven ability to author clear and compliant technical documentation, including validation protocols, test plans, and reports. Preferred Qualifications • Experience supporting aseptic fill‑finish operations and validation of vial filling lines and aseptic manufacturing technologies is preferred., • Strong organizational, analytical, and problem‑solving skills., • Strong verbal and written communication skills, including the ability to effectively present validation strategies and outcomes., • Demonstrated ability to work independently and effectively within cross‑functional teams., • Experience using project management and documentation tools (e.g., Microsoft Project, Visio, Microsoft Office) is a plus., • Willingness to work onsite as required to support manufacturing operations. Core Values The ideal candidate will embody Lantheus core values: • Let people be their best, • Respect one another and act as one, • Learn, adapt, and win, • Know someone’s health is in our hands, • Own the solution and make it happen The pay range for this position is between $89, 000 and $148,000 annually. Actual base pay offered may vary depending on a number of factors such as job-related knowledge, skills and experience. Employees in this position are eligible for a discretionary performance-based cash incentive. Benefits for this position include a comprehensive health benefits package that includes medical, prescription drug, dental, and vision coverage. Other offerings include life and disability benefits, pre-tax accounts, a 401(k) with company contribution, and a variety of other benefits. In addition, employees are eligible for a generous time off package including paid vacation, holidays, sick days, and paid parental leave. Interested candidates can apply at Lantheus.com. Applications for this position will be accepted until December 4, 2026. Lantheus is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression, sexual orientation, marital status, military service and veteran status, disability, protected medical condition as defined by applicable state or local law, genetic information, or any characteristic protected under applicable federal, state, or local laws and ordinances. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the Lantheus Talent Acquisition team at talentacquisition@lantheus.com. Lantheus is an E-Verify Employer. Applicants have rights under Federal Employment Law: Employee Polygraph Protection Act (EPPA); Family and Medical Leave Act (FMLA) For California Applicants: Family Care & Medical Leave & Pregnancy Disability Leave; California Law Prohibits Workplace Discrimination & Harassment; Your Rights and Obligations as a Pregnancy Employee For Ohio Applicants: Know Your Rights: Equal Employment Opportunity is the Law

Job Description Who we are at Osmo: Osmo is a digital olfaction company, on a mission to give computers a sense of smell to improve the health and wellbeing of human life. Why? Our sense of smell both enriches and saves lives, and has a deep and direct connection to our emotions and memory. Olfactory Intelligence has applications across industries including fragrance, manufacturing, security, medicine, and more. We believe in the power of automation and thoughtfully applied AI/ML to solve problems beyond the reach of human intuition alone. We're headquartered in Elizabeth, NJ, with an additional office in Somerville, MA. We provide complimentary shuttle service from Brooklyn and Newark, NJ. About the Role This is a ground-floor opportunity to build and lead Quality Control at Osmo. You'll own quality on both ends of the plant, raw materials coming in and finished fragrance going out, using real fragrance-industry judgment that automated testing alone can't provide. You'll have the autonomy to build the program end to end and the trust to make real-time calls from day one. What You'll Do Own Raw Material Quality — Judge incoming material results from automated testing, deciding when an out-of-spec reading is a real defect versus normal variation in a natural material. Apply Trained Olfactive Judgment — Evaluate raw materials and finished goods using olfactive evaluation the equipment can't replicate. Protect Finished Goods Quality — Run triangulation testing on outgoing product to confirm it matches prior batches before it reaches a customer. Build the QC Program — Design and continuously improve the process, documentation, and systems this function runs on, picking up from groundwork already laid. Make the Call — Decide accept or reject in real time, multiple times a day, escalating only genuinely ambiguous cases. Fix What's Broken — Spot gaps in the current process and drive the fix, rather than operating inside a system someone else already defined. Own Investigations — Lead root cause analysis on non-conforming materials, out-of-spec results, and customer quality concerns, and drive corrective actions. Run the Lab — Maintain lab documentation, SOPs, method records, and equipment calibration and qualification. Track Quality KPIs — Monitor and report on QC turnaround time, effectiveness, and recurring issues. Build the Team — Grow and lead a QC team as headcount is added. Partner Across the Floor — Work directly with Purchasing, Warehouse, Shipping and Receiving, Fragrance Development, Production, and the internal AI team on raw material and finished goods decisions. Who You Are 5+ Years in Fragrance QC — Direct fragrance industry experience required; adjacent industries like flavor, cosmetics, or specialty chemicals don't clear the bar here. 8 to 12 years is ideal. A Builder, Not Just an Operator — You've stood up or fixed a QC process before, not only executed inside one someone else built. Trained Nose — Organoleptic and sensory evaluation skill specific to fragrance raw materials and finished goods. Independent Decision-Maker — Comfortable making high-frequency accept or reject calls without over-escalating routine judgment. Quality Systems Fluent — Working knowledge of quality documentation, audits, and CAPA/root cause processes in a regulated manufacturing environment. Direct Communicator — Low-bureaucracy, thrives in a fast-moving, still-being-built environment. Technical Degree Preferred — Bachelor's in Chemistry, Chemical Engineering, or a related scientific field preferred; equivalent hands-on experience accepted in place of a degree. On Site in Elizabeth, NJ — In the plant 5 days a week. What Success Looks Like (First 6-12 Months) Establish a real, working quality QC program from a process and systems standpoint, building on the groundwork already started. Qualify raw materials at scale. Get product to customers cleanly and consistently, without holds or rejections after the fact. What We Offer (Full Time Roles Only) Ground-Floor Ownership — Build a quality function from the foundation up, not maintain someone else's finished system. Real Growth Path — Room to grow into a Director of QC role as Osmo scales to multiple sites, with potential to grow the function into a broader quality department. Catered Lunch — Mon/Wed/Fri; NJ and Brooklyn shuttles 401(k) savings plan and employer match Competitive salary and meaningful equity in a high-growth company Flexible PTO and paid family leave Commuter benefits (pre-tax transit and parking) If this role inspires you we’d encourage you to apply. We are committed to recruiting, developing, and retaining an incredible team optimized for a diversity of thought, background, and approaches. For all Full-Time Employees, compensation is just one component of Osmo’s total rewards approach, which is designed to support the well-being, growth, and long-term success of our team members. Depending on the role, this may include base salary or contract-based pay, along with access to health, dental, and vision coverage; a 401(k) retirement savings plan with company match; flexible paid time off and company holidays; and equity or incentive compensation for eligible roles. Actual compensation will vary based on factors such as experience, skills, location, internal equity, and other relevant business considerations. Osmo regularly reviews pay ranges and compensation structures to ensure they remain competitive, equitable, and aligned with current market data. All employment decisions and responsibilities are determined based on current ability and your ability to grow, without regard to race, color, gender identity, sex, sexual orientation, religion, age, marital status, physical, mental, or sensory disability, or any other characteristic protected by applicable law. Recruitment & Staffing Agencies: Osmo does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Osmo or its employees is strictly prohibited unless contacted directly by the Osmo Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Osmo and Osmo will not owe any referral or other fees with respect thereto. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire Compensation Range: $105K - $140K

Job Description Who we are at Osmo: Osmo is a digital olfaction company, on a mission to give computers a sense of smell to improve the health and wellbeing of human life. Why? Our sense of smell both enriches and saves lives, and has a deep and direct connection to our emotions and memory. Olfactory Intelligence has applications across industries including fragrance, manufacturing, security, medicine, and more. We believe in the power of automation and thoughtfully applied AI/ML to solve problems beyond the reach of human intuition alone. We're headquartered in Elizabeth, NJ, with an additional office in Somerville, MA. We provide complimentary shuttle service from Brooklyn and Newark, NJ. About the Role This is a ground-floor opportunity to build and lead Quality Control at Osmo. You'll own quality on both ends of the plant, raw materials coming in and finished fragrance going out, using real fragrance-industry judgment that automated testing alone can't provide. You'll have the autonomy to build the program end to end and the trust to make real-time calls from day one. What You'll Do Own Raw Material Quality — Judge incoming material results from automated testing, deciding when an out-of-spec reading is a real defect versus normal variation in a natural material. Apply Trained Olfactive Judgment — Evaluate raw materials and finished goods using olfactive evaluation the equipment can't replicate. Protect Finished Goods Quality — Run triangulation testing on outgoing product to confirm it matches prior batches before it reaches a customer. Build the QC Program — Design and continuously improve the process, documentation, and systems this function runs on, picking up from groundwork already laid. Make the Call — Decide accept or reject in real time, multiple times a day, escalating only genuinely ambiguous cases. Fix What's Broken — Spot gaps in the current process and drive the fix, rather than operating inside a system someone else already defined. Own Investigations — Lead root cause analysis on non-conforming materials, out-of-spec results, and customer quality concerns, and drive corrective actions. Run the Lab — Maintain lab documentation, SOPs, method records, and equipment calibration and qualification. Track Quality KPIs — Monitor and report on QC turnaround time, effectiveness, and recurring issues. Build the Team — Grow and lead a QC team as headcount is added. Partner Across the Floor — Work directly with Purchasing, Warehouse, Shipping and Receiving, Fragrance Development, Production, and the internal AI team on raw material and finished goods decisions. Who You Are 5+ Years in Fragrance QC — Direct fragrance industry experience required; adjacent industries like flavor, cosmetics, or specialty chemicals don't clear the bar here. 8 to 12 years is ideal. A Builder, Not Just an Operator — You've stood up or fixed a QC process before, not only executed inside one someone else built. Trained Nose — Organoleptic and sensory evaluation skill specific to fragrance raw materials and finished goods. Independent Decision-Maker — Comfortable making high-frequency accept or reject calls without over-escalating routine judgment. Quality Systems Fluent — Working knowledge of quality documentation, audits, and CAPA/root cause processes in a regulated manufacturing environment. Direct Communicator — Low-bureaucracy, thrives in a fast-moving, still-being-built environment. Technical Degree Preferred — Bachelor's in Chemistry, Chemical Engineering, or a related scientific field preferred; equivalent hands-on experience accepted in place of a degree. On Site in Elizabeth, NJ — In the plant 5 days a week. What Success Looks Like (First 6-12 Months) Establish a real, working quality QC program from a process and systems standpoint, building on the groundwork already started. Qualify raw materials at scale. Get product to customers cleanly and consistently, without holds or rejections after the fact. What We Offer (Full Time Roles Only) Ground-Floor Ownership — Build a quality function from the foundation up, not maintain someone else's finished system. Real Growth Path — Room to grow into a Director of QC role as Osmo scales to multiple sites, with potential to grow the function into a broader quality department. Catered Lunch — Mon/Wed/Fri; NJ and Brooklyn shuttles 401(k) savings plan and employer match Competitive salary and meaningful equity in a high-growth company Flexible PTO and paid family leave Commuter benefits (pre-tax transit and parking) If this role inspires you we’d encourage you to apply. We are committed to recruiting, developing, and retaining an incredible team optimized for a diversity of thought, background, and approaches. For all Full-Time Employees, compensation is just one component of Osmo’s total rewards approach, which is designed to support the well-being, growth, and long-term success of our team members. Depending on the role, this may include base salary or contract-based pay, along with access to health, dental, and vision coverage; a 401(k) retirement savings plan with company match; flexible paid time off and company holidays; and equity or incentive compensation for eligible roles. Actual compensation will vary based on factors such as experience, skills, location, internal equity, and other relevant business considerations. Osmo regularly reviews pay ranges and compensation structures to ensure they remain competitive, equitable, and aligned with current market data. All employment decisions and responsibilities are determined based on current ability and your ability to grow, without regard to race, color, gender identity, sex, sexual orientation, religion, age, marital status, physical, mental, or sensory disability, or any other characteristic protected by applicable law. Recruitment & Staffing Agencies: Osmo does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Osmo or its employees is strictly prohibited unless contacted directly by the Osmo Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Osmo and Osmo will not owe any referral or other fees with respect thereto. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire Compensation Range: $105K - $140K

Job Description Who we are at Osmo: Osmo is a digital olfaction company, on a mission to give computers a sense of smell to improve the health and wellbeing of human life. Why? Our sense of smell both enriches and saves lives, and has a deep and direct connection to our emotions and memory. Olfactory Intelligence has applications across industries including fragrance, manufacturing, security, medicine, and more. We believe in the power of automation and thoughtfully applied AI/ML to solve problems beyond the reach of human intuition alone. We're headquartered in Elizabeth, NJ, with an additional office in Somerville, MA. We provide complimentary shuttle service from Brooklyn and Newark, NJ. About the Role This is a ground-floor opportunity to build and lead Quality Control at Osmo. You'll own quality on both ends of the plant, raw materials coming in and finished fragrance going out, using real fragrance-industry judgment that automated testing alone can't provide. You'll have the autonomy to build the program end to end and the trust to make real-time calls from day one. What You'll Do Own Raw Material Quality — Judge incoming material results from automated testing, deciding when an out-of-spec reading is a real defect versus normal variation in a natural material. Apply Trained Olfactive Judgment — Evaluate raw materials and finished goods using olfactive evaluation the equipment can't replicate. Protect Finished Goods Quality — Run triangulation testing on outgoing product to confirm it matches prior batches before it reaches a customer. Build the QC Program — Design and continuously improve the process, documentation, and systems this function runs on, picking up from groundwork already laid. Make the Call — Decide accept or reject in real time, multiple times a day, escalating only genuinely ambiguous cases. Fix What's Broken — Spot gaps in the current process and drive the fix, rather than operating inside a system someone else already defined. Own Investigations — Lead root cause analysis on non-conforming materials, out-of-spec results, and customer quality concerns, and drive corrective actions. Run the Lab — Maintain lab documentation, SOPs, method records, and equipment calibration and qualification. Track Quality KPIs — Monitor and report on QC turnaround time, effectiveness, and recurring issues. Build the Team — Grow and lead a QC team as headcount is added. Partner Across the Floor — Work directly with Purchasing, Warehouse, Shipping and Receiving, Fragrance Development, Production, and the internal AI team on raw material and finished goods decisions. Who You Are 5+ Years in Fragrance QC — Direct fragrance industry experience required; adjacent industries like flavor, cosmetics, or specialty chemicals don't clear the bar here. 8 to 12 years is ideal. A Builder, Not Just an Operator — You've stood up or fixed a QC process before, not only executed inside one someone else built. Trained Nose — Organoleptic and sensory evaluation skill specific to fragrance raw materials and finished goods. Independent Decision-Maker — Comfortable making high-frequency accept or reject calls without over-escalating routine judgment. Quality Systems Fluent — Working knowledge of quality documentation, audits, and CAPA/root cause processes in a regulated manufacturing environment. Direct Communicator — Low-bureaucracy, thrives in a fast-moving, still-being-built environment. Technical Degree Preferred — Bachelor's in Chemistry, Chemical Engineering, or a related scientific field preferred; equivalent hands-on experience accepted in place of a degree. On Site in Elizabeth, NJ — In the plant 5 days a week. What Success Looks Like (First 6-12 Months) Establish a real, working quality QC program from a process and systems standpoint, building on the groundwork already started. Qualify raw materials at scale. Get product to customers cleanly and consistently, without holds or rejections after the fact. What We Offer (Full Time Roles Only) Ground-Floor Ownership — Build a quality function from the foundation up, not maintain someone else's finished system. Real Growth Path — Room to grow into a Director of QC role as Osmo scales to multiple sites, with potential to grow the function into a broader quality department. Catered Lunch — Mon/Wed/Fri; NJ and Brooklyn shuttles 401(k) savings plan and employer match Competitive salary and meaningful equity in a high-growth company Flexible PTO and paid family leave Commuter benefits (pre-tax transit and parking) If this role inspires you we’d encourage you to apply. We are committed to recruiting, developing, and retaining an incredible team optimized for a diversity of thought, background, and approaches. For all Full-Time Employees, compensation is just one component of Osmo’s total rewards approach, which is designed to support the well-being, growth, and long-term success of our team members. Depending on the role, this may include base salary or contract-based pay, along with access to health, dental, and vision coverage; a 401(k) retirement savings plan with company match; flexible paid time off and company holidays; and equity or incentive compensation for eligible roles. Actual compensation will vary based on factors such as experience, skills, location, internal equity, and other relevant business considerations. Osmo regularly reviews pay ranges and compensation structures to ensure they remain competitive, equitable, and aligned with current market data. All employment decisions and responsibilities are determined based on current ability and your ability to grow, without regard to race, color, gender identity, sex, sexual orientation, religion, age, marital status, physical, mental, or sensory disability, or any other characteristic protected by applicable law. Recruitment & Staffing Agencies: Osmo does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Osmo or its employees is strictly prohibited unless contacted directly by the Osmo Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Osmo and Osmo will not owe any referral or other fees with respect thereto. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire Compensation Range: $105K - $140K

Job Description Who we are at Osmo: Osmo is a digital olfaction company, on a mission to give computers a sense of smell to improve the health and wellbeing of human life. Why? Our sense of smell both enriches and saves lives, and has a deep and direct connection to our emotions and memory. Olfactory Intelligence has applications across industries including fragrance, manufacturing, security, medicine, and more. We believe in the power of automation and thoughtfully applied AI/ML to solve problems beyond the reach of human intuition alone. We're headquartered in Elizabeth, NJ, with an additional office in Somerville, MA. We provide complimentary shuttle service from Brooklyn and Newark, NJ. About the Role This is a ground-floor opportunity to build and lead Quality Control at Osmo. You'll own quality on both ends of the plant, raw materials coming in and finished fragrance going out, using real fragrance-industry judgment that automated testing alone can't provide. You'll have the autonomy to build the program end to end and the trust to make real-time calls from day one. What You'll Do Own Raw Material Quality — Judge incoming material results from automated testing, deciding when an out-of-spec reading is a real defect versus normal variation in a natural material. Apply Trained Olfactive Judgment — Evaluate raw materials and finished goods using olfactive evaluation the equipment can't replicate. Protect Finished Goods Quality — Run triangulation testing on outgoing product to confirm it matches prior batches before it reaches a customer. Build the QC Program — Design and continuously improve the process, documentation, and systems this function runs on, picking up from groundwork already laid. Make the Call — Decide accept or reject in real time, multiple times a day, escalating only genuinely ambiguous cases. Fix What's Broken — Spot gaps in the current process and drive the fix, rather than operating inside a system someone else already defined. Own Investigations — Lead root cause analysis on non-conforming materials, out-of-spec results, and customer quality concerns, and drive corrective actions. Run the Lab — Maintain lab documentation, SOPs, method records, and equipment calibration and qualification. Track Quality KPIs — Monitor and report on QC turnaround time, effectiveness, and recurring issues. Build the Team — Grow and lead a QC team as headcount is added. Partner Across the Floor — Work directly with Purchasing, Warehouse, Shipping and Receiving, Fragrance Development, Production, and the internal AI team on raw material and finished goods decisions. Who You Are 5+ Years in Fragrance QC — Direct fragrance industry experience required; adjacent industries like flavor, cosmetics, or specialty chemicals don't clear the bar here. 8 to 12 years is ideal. A Builder, Not Just an Operator — You've stood up or fixed a QC process before, not only executed inside one someone else built. Trained Nose — Organoleptic and sensory evaluation skill specific to fragrance raw materials and finished goods. Independent Decision-Maker — Comfortable making high-frequency accept or reject calls without over-escalating routine judgment. Quality Systems Fluent — Working knowledge of quality documentation, audits, and CAPA/root cause processes in a regulated manufacturing environment. Direct Communicator — Low-bureaucracy, thrives in a fast-moving, still-being-built environment. Technical Degree Preferred — Bachelor's in Chemistry, Chemical Engineering, or a related scientific field preferred; equivalent hands-on experience accepted in place of a degree. On Site in Elizabeth, NJ — In the plant 5 days a week. What Success Looks Like (First 6-12 Months) Establish a real, working quality QC program from a process and systems standpoint, building on the groundwork already started. Qualify raw materials at scale. Get product to customers cleanly and consistently, without holds or rejections after the fact. What We Offer (Full Time Roles Only) Ground-Floor Ownership — Build a quality function from the foundation up, not maintain someone else's finished system. Real Growth Path — Room to grow into a Director of QC role as Osmo scales to multiple sites, with potential to grow the function into a broader quality department. Catered Lunch — Mon/Wed/Fri; NJ and Brooklyn shuttles 401(k) savings plan and employer match Competitive salary and meaningful equity in a high-growth company Flexible PTO and paid family leave Commuter benefits (pre-tax transit and parking) If this role inspires you we’d encourage you to apply. We are committed to recruiting, developing, and retaining an incredible team optimized for a diversity of thought, background, and approaches. For all Full-Time Employees, compensation is just one component of Osmo’s total rewards approach, which is designed to support the well-being, growth, and long-term success of our team members. Depending on the role, this may include base salary or contract-based pay, along with access to health, dental, and vision coverage; a 401(k) retirement savings plan with company match; flexible paid time off and company holidays; and equity or incentive compensation for eligible roles. Actual compensation will vary based on factors such as experience, skills, location, internal equity, and other relevant business considerations. Osmo regularly reviews pay ranges and compensation structures to ensure they remain competitive, equitable, and aligned with current market data. All employment decisions and responsibilities are determined based on current ability and your ability to grow, without regard to race, color, gender identity, sex, sexual orientation, religion, age, marital status, physical, mental, or sensory disability, or any other characteristic protected by applicable law. Recruitment & Staffing Agencies: Osmo does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Osmo or its employees is strictly prohibited unless contacted directly by the Osmo Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Osmo and Osmo will not owe any referral or other fees with respect thereto. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire Compensation Range: $105K - $140K

Job Description Company introduction: Compass Pathways plc (Nasdaq: CMPS) is a biotechnology company dedicated to unlocking urgently needed new treatment options in mental health care. The Company is headquartered in London, UK, with a U.S. office in New Jersey. We believe mental health patients deserve the possibility of a better future. Our initial focus is developing COMP360 psilocybin, a proprietary, investigational, synthetic psilocybin treatment under evaluation for treatment-resistant depression (TRD) and post-traumatic stress disorder (PTSD). COMP360 is a potentially first-in-class treatment and has Breakthrough Therapy designation from the U.S. Food and Drug Administration (FDA), as well as Innovative Licensing and Access Pathway (ILAP) designation in the UK for TRD. We are leading the world's largest classic psychedelic clinical program in TRD, and building upon that robust foundation, we are executing a late-stage trial evaluating COMP360 for PTSD, another condition with high unmet need. Our goal is to advance treatments that move the field of psychiatry towards treatment options that offer rapid onset and sustained durability with infrequent dosing. - Compass Pathways Job overview: The Patient Access Liaison (PAL) is responsible for site-level execution of Compass Pathways' patient engagement strategy by supporting REMS certification, strengthening site access readiness, and providing compliant coverage and reimbursement education to healthcare stakeholders. The PAL serves as a field-based patient access resource who helps sites understand treatment logistics, identify information gaps, address patient access barriers, and support operational readiness across REMS requirements, specialty pharmacy, distribution, and external support processes. In addition, the PAL strengthens account and stakeholder relationships, collaborates appropriately with matrix team members, maintains disciplined CRM documentation, and upholds non-promotional role boundaries. This role also shares recurring field insights and process-improvement opportunities. Location: Field based in Newark, NJ or Frederick, MD. Reports to: Regional Director, Field Patient Access. Roles and Responsibilities (include but are not limited to): • Support REMS certification and enrolment: Educate sites on REMS site certification activities and patient REMS enrolment processes, including applicable operational, requirements, • Enable site access readiness: Support site access workflows following REMS certification, strengthen account and stakeholder relationships, and help ensure operational readiness for therapy delivery while streamlining the patient journey, • Provide reimbursement and access education: Provide compliant and proactive education to site and office personnel regarding coverage, coding, payment, reimbursement, benefit investigations, claims, prior authorizations, appeals, and access processes, • Educate on case management processes: Educate on appropriate case management processes for consented patients, including compliant use of patient healthcare information, benefit investigations, benefit verifications, prior authorizations, appeals, and affordability program navigation, • Support case-level access resolution: Identify, troubleshoot, case-level access barriers through appropriate buy-and-bill, specialty pharmacy, HUB, and other approved support pathways, • Enable treatment logistics understanding: Coordinate patient treatment logistics and scheduling across REMS requirements, HUB, specialty pharmacies, distribution partners, and other external support networks, • Collaborate on cross-functional handoffs: Receive and act upon referrals and handoffs from Sales and Site of Care Account Leads regarding site readiness, account economics discussions, and case-level access challenges, • Maintain compliant documentation: Maintain accurate, compliant, and timely documentation of account activities, case interactions, and resolution outcomes within the CRM system to support cross-functional visibility and coordination, • Manage accounts and maintain business plans: Develop, maintain, and execute account-level business plans that reflect site access priorities, stakeholder needs, operational readiness, and patient access opportunities within the assigned geography, • Maintain non-promotional role boundaries: Refrain from engaging in promotional activities, product promotion, or commercial sales discussions Candidate Profile: • Experience: Candidate must have a minimum of 3 years of experience in field reimbursement, patient access, and case management within pharmaceutical, biotechnology, specialty healthcare, including required experience navigating a healthcare ecosystem, • Industry Knowledge:, • Access & Reimbursement Expertise: Candidate must have experience supporting access and reimbursement processes, specialty pharmacy programs, patient support services, coverage, benefit verification, prior authorization, appeals, affordability programs, and compliant access resources, • Patient Journey Enablement: Candidate must have experience helping sites and stakeholders support patient progression from referral through treatment initiation by identifying barriers, connecting resources, and reinforcing treatment readiness and next steps, • Strategic Account Support: Candidate must have experience partnering with treatment sites to assess needs, strengthen workflows, build trusted account and stakeholder relationships, • Operational Excellence & Execution: Candidate must demonstrate strong planning, organization, accountability, disciplined execution, and the ability to use data and field insights to anticipate and address access challenges across multiple accounts and priorities, • Collaborative Influence & Compliance: Candidate must have experience collaborating compliantly with matrix partners while maintaining appropriate role boundaries, communicating access barriers and field insights, and balancing stakeholder needs with patient-centered execution, • Education: Bachelor's degree required, • Certifications and licenses: Valid driver's license required, • Travel: Ability and willingness to travel within an assigned geography, including travel by air and car, with travel estimated to be 50% or more. Candidate must reside within 25 miles of the assigned territory border(s). Assigned geography may be larger at launch and may evolve or become more focused as the field organization expands Compensation Description (annually): Our compensation package for permanent hires includes base salary, discretionary bonus, and equity, alongside our comprehensive benefits offering. Please note that the base salary range is a guideline, and individual total compensation will vary based on factors such as qualifications, skill level, competencies, and work location. 【Base salary per annum】: $180,000—$200,000 USD Benefits: For an overview of our benefits package and compensation information, please visit "Joins us - Our Benefits". These include flexibility & generous time off, parental & reproductive support, health & medical, mental health & wellbeing and Financial health. Equal opportunities: Reasonable accommodation We are committed to building a workplace where everyone's wellbeing matters. If you need reasonable accommodation during the interview process to be at your best, please let our recruiting team know. UK applicants We are proud of our commitment to diversity and equality (pursuant to the Equality Act 2010). We do not discriminate based upon race, religion or belief, colour, nationality, ethnic or national origin, gender, pregnancy or maternity, marital or civil partner status, sexual orientation, gender reassignment, age or disability. US applicants Compass Pathways is proud to be an equal opportunity employer. All employment decisions are based on business needs, job requirements, and individual qualifications, without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, and related medical conditions), ethnicity, age, disability, sexual orientation, gender identity, gender expression, military service, genetic information, familial or marital status, or any other status, category, or characteristic protected by applicable law. Sponsorship: Unfortunately, we cannot sponsor employment visas and can only accept applications if you have employment rights in the country to which you are applying. Data Privacy: All data is confidential and protected by all legal and data privacy requirements, please see our recruitment Privacy Notice to learn more about how we process personal data.

Job Description Who we are at Osmo: Osmo is a digital olfaction company, on a mission to give computers a sense of smell to improve the health and wellbeing of human life. Why? Our sense of smell both enriches and saves lives, and has a deep and direct connection to our emotions and memory. Olfactory Intelligence has applications across industries including fragrance, manufacturing, security, medicine, and more. We believe in the power of automation and thoughtfully applied AI/ML to solve problems beyond the reach of human intuition alone. We're headquartered in Elizabeth, NJ, with an additional office in Somerville, MA. We provide complimentary shuttle service from Brooklyn and Newark, NJ. About the Role This is a ground-floor opportunity to build and lead Quality Control at Osmo. You'll own quality on both ends of the plant, raw materials coming in and finished fragrance going out, using real fragrance-industry judgment that automated testing alone can't provide. You'll have the autonomy to build the program end to end and the trust to make real-time calls from day one. What You'll Do Own Raw Material Quality — Judge incoming material results from automated testing, deciding when an out-of-spec reading is a real defect versus normal variation in a natural material. Apply Trained Olfactive Judgment — Evaluate raw materials and finished goods using olfactive evaluation the equipment can't replicate. Protect Finished Goods Quality — Run triangulation testing on outgoing product to confirm it matches prior batches before it reaches a customer. Build the QC Program — Design and continuously improve the process, documentation, and systems this function runs on, picking up from groundwork already laid. Make the Call — Decide accept or reject in real time, multiple times a day, escalating only genuinely ambiguous cases. Fix What's Broken — Spot gaps in the current process and drive the fix, rather than operating inside a system someone else already defined. Own Investigations — Lead root cause analysis on non-conforming materials, out-of-spec results, and customer quality concerns, and drive corrective actions. Run the Lab — Maintain lab documentation, SOPs, method records, and equipment calibration and qualification. Track Quality KPIs — Monitor and report on QC turnaround time, effectiveness, and recurring issues. Build the Team — Grow and lead a QC team as headcount is added. Partner Across the Floor — Work directly with Purchasing, Warehouse, Shipping and Receiving, Fragrance Development, Production, and the internal AI team on raw material and finished goods decisions. Who You Are 5+ Years in Fragrance QC — Direct fragrance industry experience required; adjacent industries like flavor, cosmetics, or specialty chemicals don't clear the bar here. 8 to 12 years is ideal. A Builder, Not Just an Operator — You've stood up or fixed a QC process before, not only executed inside one someone else built. Trained Nose — Organoleptic and sensory evaluation skill specific to fragrance raw materials and finished goods. Independent Decision-Maker — Comfortable making high-frequency accept or reject calls without over-escalating routine judgment. Quality Systems Fluent — Working knowledge of quality documentation, audits, and CAPA/root cause processes in a regulated manufacturing environment. Direct Communicator — Low-bureaucracy, thrives in a fast-moving, still-being-built environment. Technical Degree Preferred — Bachelor's in Chemistry, Chemical Engineering, or a related scientific field preferred; equivalent hands-on experience accepted in place of a degree. On Site in Elizabeth, NJ — In the plant 5 days a week. What Success Looks Like (First 6-12 Months) Establish a real, working quality QC program from a process and systems standpoint, building on the groundwork already started. Qualify raw materials at scale. Get product to customers cleanly and consistently, without holds or rejections after the fact. What We Offer (Full Time Roles Only) Ground-Floor Ownership — Build a quality function from the foundation up, not maintain someone else's finished system. Real Growth Path — Room to grow into a Director of QC role as Osmo scales to multiple sites, with potential to grow the function into a broader quality department. Catered Lunch — Mon/Wed/Fri; NJ and Brooklyn shuttles 401(k) savings plan and employer match Competitive salary and meaningful equity in a high-growth company Flexible PTO and paid family leave Commuter benefits (pre-tax transit and parking) If this role inspires you we’d encourage you to apply. We are committed to recruiting, developing, and retaining an incredible team optimized for a diversity of thought, background, and approaches. For all Full-Time Employees, compensation is just one component of Osmo’s total rewards approach, which is designed to support the well-being, growth, and long-term success of our team members. Depending on the role, this may include base salary or contract-based pay, along with access to health, dental, and vision coverage; a 401(k) retirement savings plan with company match; flexible paid time off and company holidays; and equity or incentive compensation for eligible roles. Actual compensation will vary based on factors such as experience, skills, location, internal equity, and other relevant business considerations. Osmo regularly reviews pay ranges and compensation structures to ensure they remain competitive, equitable, and aligned with current market data. All employment decisions and responsibilities are determined based on current ability and your ability to grow, without regard to race, color, gender identity, sex, sexual orientation, religion, age, marital status, physical, mental, or sensory disability, or any other characteristic protected by applicable law. Recruitment & Staffing Agencies: Osmo does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Osmo or its employees is strictly prohibited unless contacted directly by the Osmo Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Osmo and Osmo will not owe any referral or other fees with respect thereto. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire Compensation Range: $105K - $140K

Job Description Position Overview: The Director of Safety is responsible for leading and managing the company’s safety and regulatory compliance programs across a fleet of approximately 500 trucks. This position oversees DOT and FMCSA compliance, driver safety, accident prevention and investigation, fleet safety technology, training, and risk management. The Director of Safety will establish a proactive safety culture, minimize accidents and financial losses, and ensure consistent safety standards across all operating locations. Working closely with executive leadership, operations, maintenance, dispatch, human resources, and insurance partners, this role will use safety data, performance metrics, and corrective action plans to improve fleet safety, maintain regulatory compliance, and protect drivers, the public, company assets, and customers. Essential Job Functions • Develop, implement, and enforce company-wide safety policies, procedures, and performance standards., • Ensure compliance with applicable DOT, FMCSA, state regulations, hours-of-service requirements, ELDs, driver qualification files, CDL requirements, and drug and alcohol testing programs., • Monitor CSA performance, roadside inspections, regulatory changes, and compliance trends; coordinate audits, inspections, and corrective actions., • Oversee driver onboarding, qualification, orientation, safety training, coaching, and performance management., • Utilize telematics, dash cameras, ELDs, and other safety technologies to identify risk and improve driver performance., • Lead accident and incident reporting, investigations, preventability reviews, claims coordination, and root-cause analysis., • Partner with fleet maintenance to ensure vehicle inspections, safety defects, and equipment-related violations are addressed promptly., • Conduct internal safety audits and ensure corrective actions are documented, completed, and verified., • Establish and monitor key performance indicators related to accidents, violations, compliance, training, claims, and overall safety performance., • Provide regular safety reports, trend analysis, and improvement recommendations to executive leadership., • Lead and develop the safety team while collaborating with terminal managers, operations, dispatch, maintenance, recruiting, and human resources., • Promote a culture of accountability, continuous improvement, and consistent adherence to safety standards across all locations., • Ensure safety requirements are maintained without compromise to delivery schedules or productivity objectives., • Conduct all business in a highly ethical manner, exhibiting behavior, practices, and standards that uphold IMC core values., • Perform other duties as assigned. Job Requirement • Bachelor’s degree in safety management, transportation, business administration, or a related field preferred; equivalent relevant experience may be considered., • 7+ years of experience, prior senior safety leadership, and relevant professional certifications preferred., • 5+ years of progressive experience in trucking safety, transportation compliance, fleet risk management, or a related field., • Demonstrated experience managing safety programs for a large commercial trucking fleet; experience with 300–500 or more trucks strongly preferred., • Strong working knowledge of DOT and FMCSA regulations, driver qualification requirements, hours-of-service compliance, and commercial vehicle safety., • Experience with accident investigations, claims management, regulatory audits, and corrective action programs., • Ability to analyze safety data, identify trends, and implement measurable performance improvements., • Experience with ELDs, fleet telematics, safety monitoring systems, and reporting tools., • Strong leadership, communication, organizational, analytical, and problem-solving skills., • Ability to manage multiple locations, competing priorities, and time-sensitive safety issues., • Experience working with commercial auto insurers, claims adjusters, and transportation legal counsel preferred., • Availability to travel to terminals, operating locations, accident scenes, and regulatory or insurance meetings as needed., • Availability outside normal business hours to respond to serious accidents, emergencies, or critical compliance issues. Other Skills / Abilities • A Strong safety leadership, sound judgment, and commitment to regulatory compliance., • Effective driver coaching, accident investigation, and root-cause analysis skills., • Ability to interpret safety data and develop actionable performance improvement plans., • Strong cross-functional collaboration and relationship-building skills., • Proficiency with Microsoft Office Suite and related fleet safety and reporting systems., • Ability to prioritize risks, maintain accurate documentation, and ensure timely follow-through., • Commitment to ethical conduct, employee accountability, and a safe working environment. Work Location: This position will cover 2 Regions - Ohio Valley and North Atlantic

Job Description The Site Safety & Compliance Lead serves as the senior safety representative for an assigned market, creating a safe, compliant, and operationally sound workplace. Reporting to the Director of Mobility Safety, this role leads environmental health and safety compliance, employee safety, incident and injury management, emergency preparedness, operational assurance, and local safety-culture efforts. The position works closely with employees and local leaders to identify and correct hazards, reinforce safe work and driving practices, and apply Just Culture and Safety Management System principles across fleet operations. A Day in the Life: No two days are the same. You may begin by walking the site and addressing an employee safety concern, then coach a driver on safe behaviors, review an incident and supporting video, or coordinate care for an injured employee. Throughout the day, you will partner with local leaders, track corrective actions, monitor regulatory and operational compliance, prepare teams for emergencies, and deliver practical safety training. Your visible presence and sound judgment will help employees feel supported while strengthening accountability and a proactive safety culture. The salary range for this position is $95,000-$120,000 What You’ll Do: • Serve as the primary on-site resource for employee safety concerns; investigate, resolve, and document issues in the Safety Management System, • Provide real-time coaching on safe work practices and driving behaviors, and champion local safety campaigns, committees, and toolbox talks, • Conduct routine site inspections, verify PPE compliance, identify hazards, and track corrective actions through closure, • Manage workplace injuries and illnesses, coordinate medical care and workers’ compensation cases, support OSHA recordkeeping, and ensure first-aid readiness, • Coordinate spill response, environmental permits, waste handling, and compliance with established EHS policies and standards, • Lead or oversee minor and moderate incident investigations, preserve evidence, review video and facts, identify contributing factors, and ensure objective documentation and closure, • Develop local emergency plans and maps; lead drills; maintain emergency equipment; train employees; and coordinate with first responders during events, • Conduct operational compliance audits, identify process gaps, monitor telematics and driver-coaching compliance, and escalate safety or quality risks, • Deliver ongoing safety training, promote hazard and near-miss reporting, and validate safety knowledge before employees begin independent work What We’re Looking For: • Associate’s or bachelor’s degree in Occupational Safety, Environmental Science, or a related field, or equivalent experience, • Five or more years of EHS experience in transportation, logistics, fleet operations, manufacturing, or a similar multi-site environment, • Strong knowledge of OSHA regulations including 29 CFR 1910, recordkeeping, injury reporting, workplace inspections, and emergency action plans, • Experience managing workplace injuries, workers’ compensation, return-to-work processes, and incident investigations, • Experience conducting operational compliance or quality audits and translating findings into practical corrective actions, • Strong safety leadership, coaching, communication, and interpersonal skills, with the ability to influence employees and supervisors without formal authority, • Emergency-response experience, including drills, emergency-plan execution, and coordination with first responders, • Ability to work independently, prioritize competing demands, exercise sound judgment, and escalate appropriately, • Proficiency with safety platforms and telematics tools; Samsara or a similar platform is preferred., • Preferred qualifications include OSHA 30-Hour, ASP, First Aid/CPR, emergency-management, or equivalent certifications; familiarity with SMS or ISO 45001; fleet or mobility-industry experience; and bilingual capability relevant to the market What You’ll Get: • Paid Time Off, • Medical, Dental & Vision plan options, • Retirement programs, including 401(k) employer matching, • Paid Parental Leave & Adoption Assistance, • Employee Assistance Program for employees & family, • Educational Reimbursement & Discounts, • Voluntary Insurance Programs - Pet, Legal/Identity Theft, Critical Illness, • Perks & Discounts –Theme Park Tickets, Gym Discounts & more #ORO #ZR

Are you a current NJIT employee? Apply.The Research Analyst will conduct experiments on contamination in soils and water for projects led by the CNR and assist the Director of the CNR in the implementation.Conduct experiments on contamination in soils and water.Laboratory and field investigations in

If further details of the position are needed, please contact the Police Director, Frank D'Errico. The City of Rahway Police Department, Investigations Division, is recruiting a full-time Clerk 1 employee.

Under the direction of the Risk Services Director, this position is responsible for providing risk management services and support with the essential functions under Business Insurance Program (Claim Investigation); Real Estate and Property Rights Program; and Risk Services throughout the Middlesex Water Company Enterprise. Work Performed: Business Insurance Program (Claim Investigation Program) Essential Functions: • Manage and review all Risk Reports including, but not limited to, review of completeness, root cause analysis, and corrective actions., • Coordinates investigations and remedial corrective actions with supervisory and/or Dispatch personnel in Operations., • Manage and coordinate claims with insurance company adjusters., • Manage and develop various schedules to track claims and litigation., • Assist in management and coordination of after-hour inquiries regarding claims, as needed. Real Estate and Property Rights Program Essential Functions: • Assist with inspection of Enterprise properties, right-of-ways and easements for potential hazards, damage and insurance-related requirements., • Assist with the day-to-day operations of the Real Estate Property Right Program. Risk Services - Essential Functions: • Manage and coordinate area of responsibility on the Risk Department Balanced Scorecard., • Manage and coordinate Schedule of Action Items for the Enterprise., • Attend pre-construction, project and progress meetings as needed Enterprise-wide., • Recommends modifications to existing programs and procedures to improve system reliability and reduce liability., • Contribute to the overall safety awareness throughout the Enterprise., • Assist in contingency planning and response coordination of emergency situations., • Communicate with customers, contractors, attorneys, municipalities, the general public, etc., in a responsible and courteous manner., • Work on projects/other duties as assigned by the Risk Services Director., • Assist in all areas of the Risk Department when personnel on vacation or leave. Qualifications: • High School Diploma or GED required., • Maintain a valid NJ drivers license., • At least five years of experience in the area of Transmission and Distribution operations, maintenance, construction and supervision, desired., • Ability to read, understand and use GIS, CC&B, WAM, MWM, construction plans and distribution system maps, desired., • Availability for emergency call-in and on-call assignments, as needed., • Must be able to work outdoors on a year-round basis., • Be able to work independently, with little supervision., • Strong written and verbal communication skills., • Strong analytical skills., • Proficient in Microsoft Office Suite and Adobe Acrobat Pro., • Experience with databases. Compensation & Benefits: Salary Range: $55,355 $83,034 annually, based on experience and qualifications. Total Rewards Package Includes: - Medical, dental, & vision coverage (effective first of the month after hire). 401(k) with company match. Company paid life and disability insurance. Paid time off and 12 paid holidays. Tuition assistance and professional development opportunities. Physical Requirements: • Ability to climb ladders, enter/exit confined spaces, enter/exit excavations., • Able to work outdoors in inclement weather., • Ability to bend, stoop, sit for extended periods of time., • This position requires operation of a computer and other office equipment such as printers, copiers, scanners and calculators., • Must have the ability to visually inspect and review hard copy and online documents., • Must be able to communicate, detect, converse with, discern, convey, express oneself, discuss and exchange information., • Must be able to occasionally move about inside the office and use stairs to access file cabinets, office machinery, etc., • Ability to lift and carry 25 pounds unassisted and at least 50-75 pounds assisted., • Must be able to remain in a stationary position 50 percent of the time. Work Authorization & Pre-Employment Requirements: Candidates must be authorized to work in the United States. All candidates must successfully pass a drug screen, pre-employment physical, background check, and possess a valid driver's license in good standing (if required for the position). Commercial Driver's License (CDL) Positions: For positions requiring a Commercial Driver's License (CDL), the use of marijuana (including medical marijuana) or any controlled substances, whether prescribed or otherwise, is strictly prohibited under Federal Motor Carrier Safety Administration (FMCSA) regulations of the U.S. Department of Transportation (DOT). Such use is a violation of federal law and will disqualify candidates from CDL-required positions. Pay Transparency: This job posting complies with the New Jersey Pay Transparency Law (effective June 1, 2025), which requires employers to disclose salary ranges, benefits, and other compensation in job advertisements. Recruitment Fraud Alert: We have noticed an increase in recruiting impersonations across the industry, where scammers attempt to obtain candidates' personal or financial information through fake interviews and offers. All legitimate communications from Middlesex Water Company and its subsidiaries will originate from the following email domains: @msg.clrco.com or @clearcompany.com. Any outreach claiming to be from Middlesex Water Company or its subsidiaries that does not come from these domains should be ignored. Equal Employment Opportunity: Middlesex Water Company and its subsidiaries are Equal Opportunity Employers and are committed to creating an inclusive environment for all employees. We consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, genetic information, or any other characteristic protected by applicable law. Applicant Communication: Please note: No phone calls, please. We thank all applicants in advance for their interest; however, only those selected for an interview will be contacted.

The Director, Safety, Security & Environmental (SSE) is responsible for developing leading and continuously improving the enterprise-wide strategies, programs and policies that promote a safe, secure and environmentally compliant and responsible workplace. This position provides strategic leadership for occupational safety, physical security, environmental compliance, emergency preparedness and risk management initiatives to protect employees, customers, assets and the communities we serve. This role champions a proactive, prevention-focused culture that reinforces the Company's commitment to operational excellence, regulatory compliance, and its mission of "Sustaining life with every drop." The Director partners across operations and support functions to foster a strong culture of safety, environmental stewardship and operational resilience while ensuring compliance with applicable regulations, industry standards and company's policies. This role promotes accountability and continuous improvement through the Company's guiding principle: "Think Safety, Act Safely." Reports to: Chief Operating Officer (COO) Key Responsibilities: Strategic Leadership • Develop and execute an integrated enterprise-wide SSE strategy aligned with the MWC 2030 pillars and priorities, • Serve as a trusted advisor to executive leadership on safety, environmental, security, and regulatory matters, • Lead initiatives that strengthen organizational culture, reduce operational risk, and enhance enterprise resilience, • Develop policies, standards and procedures supporting regulatory compliance and operational excellence, • Foster a culture of accountability, prevention, and continuous improvement across all business units, • Lead SSE audits and inspections and ensure timely resolution of findings, • Ensure lessons learned from incidents and exercises are incorporated into policies and procedures, • Build strong relationships with regulators, emergency responders, law enforcement, industry organizations and other stakeholders Safety • Develop and execute the company's enterprise safety strategy, policies, standards and programs, • Establish a proactive safety culture focused on prevention, accountability and continuous improvement, • Ensure compliance with OSHA and all applicable federal, state, and local safety regulations, • Lead the development, implementation, and continuous improvement of enterprise safety programs, policies, procedures, and training, • Lead incident investigations, root cause analysis activities, ensure implementation of corrective actions, and lessons learned processes, • Drive proactive hazard identification, near-miss reporting, and risk mitigation efforts, • Partner with operational leadership to embed safety into daily work practices and decision-making, • Drive behavior-based safety initiatives and continuous learning programs, • Establish and monitor safety goals, performance metrics and KPIs., • Promote employee engagement and ownership of safety at every level of the organization, • Promote a culture where safety is integrated into daily operations and decision making Environmental • Lead the company's environmental compliance programs with environmental regulations and reporting requirements, including EPA, NJDEP, DNREC, and other applicable agencies, • Support environmental due diligence associated with capital projects, acquisitions and other strategic initiatives. Oversee environmental programs related to permitting, compliance, water quality, inspections, and environmental stewardship, • Partner with Operations and Engineering to integrate environmental considerations into operational activities and capital projects, • Monitor environmental performance metrics and develop and lead initiatives that support sustainability and continuous improvement Support environmental risk assessments and mitigation activities Safety & Emergency Preparedness • Develop, maintain and Oversee physical security programs for facilities, assets, and critical infrastructure across the enterprise, • Conduct security risk assessments and vulnerability assessments of critical facilities and infrastructure, • Partner closely with IT and cybersecurity leadership on the intersection of physical security, operational technology and cybersecurity, • Establish appropriate access control, surveillance, intrusion detection, visitor management and security protocols, • Monitor emerging threats to the water sector and recommend appropriate mitigation measures, • Ensure compliance with applicable utility security standards and regulatory requirements, • Partner with IT, Operations, and leadership teams on emergency preparedness, incident response, crisis management, and business continuity planning, • Lead emergency response planning and incident management processes, • Coordinate training exercises and preparedness drills, • Identify operational risks and develop mitigation strategies, • Support business continuity and resilience efforts, • Lead response coordination and mitigation efforts related to security risks, threats, or emergency events Leadership and Team Development • Lead and develop SSE teams, • Establish performance objectives and professional development plans, • Manage department budget and resources, • Foster a collaborative and high performing team Operational Integration • Integrate SSE standards and expectations into field operations, maintenance activities, construction, and capital projects (CAPEX), • Ensure consistent application of policies, procedures, and compliance standards across all locations and operating units, • Collaborate cross-functionally to align SSE priorities with operational and business objectives Training, Communication & Culture • Develop and implement enterprise SSE training, awareness, and engagement programs, • Promote a speak-up culture centered on accountability, prevention, and employee involvement, • Lead communications and enterprise campaigns reinforcing the "Think Safety, Act Safely" philosophy, • Support leadership development and employee engagement initiatives related to SSE performance and culture Data, Reporting & Performance Management • Establish, monitor, and analyze key performance indicators (KPIs), including TRIR, DART, environmental compliance metrics, and security-related metrics, • Utilize trend analysis and data insights to identify risks and drive continuous improvement initiatives, • Prepare and present SSE performance updates, recommendations, and strategic insights to executive leadership and Board-level stakeholders Qualifications & Requirements: Required • Bachelor's degree in safety, Environmental Health, Engineering, Industrial Hygiene, or a related field, • Minimum of 15 years of progressive leadership experience in safety, environmental, security, or industrial operations, • Strong working knowledge of OSHA, EPA, and applicable state regulatory requirements, • Demonstrated leadership experience building and sustaining high-performance, compliance-focused cultures, • Strong communication, analytical, and cross-functional leadership skills, • Experience leading enterprise-wide safety and environmental programs Preferred • CSP (Certified Safety Professional), CHMM, or related professional certification, • Experience within the water, wastewater, utility, or other regulated industry environment, • Experience supporting emergency response, crisis response, business continuity, and enterprise risk management initiatives Success Measures • Reduction in safety incidents, recordable rate and lost time events, • Improvement in leading safety indicators, • Successful implementation of safety, security and environmental compliance initiatives, • Employee safety and security engagement, • Completion and effectiveness if emergency exercises, • Improved safety culture and employee engagement scores, • Strong regulatory compliance performance, • Effective emergency preparedness and response capabilities, • Enhanced environmental and sustainability outcomes Working Conditions: This is a full-time, non-exempt, in-office position. Occasional travel to other company sites may be required. Must be able to lift and transport training materials up to 25 pounds as needed. Compensation & Benefits: • Salary Range: $130,800 to $196,200 annually, based on experience and qualifications., • Total Rewards Package Includes: - Medical, dental, and vision coverage (effective first of the month after hire)., • 401(k) with company match., • Company paid life and disability insurance., • Paid time off and 12 paid holidays., • Tuition assistance and professional development opportunities. <

Job information: • · Functional title - UEBA Use Case Developer/Manager UEBA, • Department – IT Security, • Corporate level – Vice President, • Report to – Director of Insider Threat, • Location - Iselin, New Jersey, • Compensation – $143,000 - 166,000 base salary + variable compensation + 401(k) match + benefits Overview of the role: CLS is seeking a highly motivated, and skilled Vice President - UEBA (User Entity Behavioral Analysis) Use Case Developer/Manager to join our Insider Threat Team. The role will be located in New Jersey. The position will report to the Director of Insider Threat and will participate in the development, implementation, and continuous improvement of a new Insider Threat team. This role involves the identification, detection and investigation of abnormal actions from internal accounts which may be indicative of risk posed by individuals with authorized access to organizational assets, including employees and third-party vendors. The position will require collaboration with cross-functional teams to mitigate the risks of malicious, negligent, or unintentional insider actions that could lead to security breaches, data loss, or system unavailability. This position requires someone with an analytical mind and data analysis skills, working knowledge of company systems and IT security tools, a quick learner, and the ability to propose and execute on program improvements. This role will also be responsible for building relationships with organizational partners and conducting investigations. What you will be doing: • Integrate UEBA capabilities with SIEM, SOAR, EDR DLP, and IAM systems., • Establish baselines of normal user behavior across identity, network, endpoint and application activity., • Monitor user risk scores and tune detection logic to reduce false positives and improve detection fidelity, identifying and onboarding new telemetry sources., • Drive incident response and insider threat investigations with timeline and data analysis. Conduct proactive behavioral threat hunting using UEBA data., • Manage playbook response actions and support investigations of suspected insider threat incidents to include preventative controls and user quarantine actions., • Align behavioral monitoring with privacy, legal and HR considerations., • Participate in the execution of the insider threat program, including the development of tools, standards, procedures, and processes to detect, prevent, and respond to insider threats., • Research advanced detection and monitoring tools to complement existing systems., • Drive continuous improvement by integrating lessons learned, industry best practices, and emerging threat intelligence., • Collaborate with stakeholders across the firm to evaluate and address potential insider risks across systems, networks, and organizational processes., • Participate in investigations and produce reports on insider threat risks, incidents, and mitigation efforts for executives to aid in their decision making., • Work with the intelligence team to develop threat modelling deliverables, · What we’re looking for: Experience • 8+ years of experience in information security such as Insider Threat, Investigations, Analysis, Security Operations, Incident Response, or Threat Intelligence roles., • Experience with insider threat detection tools (UEBA, SIEM, EDR, DLP) and knowledge of advanced threat intelligence techniques., • 3+ years of experience in Insider Threat or equivalent., • Knowledge of fundamentals of threat actors’ TTPs and MITRE ATT&CK Framework., • Understanding of security frameworks, incident response, and risk management practice., • Knowledge of relevant legal and regulatory considerations, including privacy laws and data protection requirements., • Excellent interpersonal and relationship management skills. Professional qualifications / certifications • Bachelor’s Degree in Cybersecurity studies, Information Systems, Computer Science, Business Analytics, Intelligence Studies, Criminology, or related discipline., • Experience or the ability to operate & tune security monitoring and analytical tools (e.g. UEBA, SIEM, EDR, DLP) is highly preferred., • Expertise in managing initial incident response and supporting investigations, coordinating with multiple departments, and resolving security incidents efficiently., • Security certification through a credentialing organization which demonstrates knowledge of cybersecurity, defense, vulnerabilities, data and operating system security e.g. SANS, ISC2, ISACA., • Experience with threat intelligence and SOC/CIRT interaction., • Experience in handling sensitive information., • Strong written and verbal communication skills as well as interview skills., • Ability to work on-site at least twice a week in New Jersey and/or participate in local intelligence sharing groups., • Financial sector experience.

Job Description Core Duties & Guest Experience Serves as the first point of contact, warmly greeting and assisting patients, guests, and staff with a high standard of courtesy and professionalism. Elevates the overall guest experience by proactively offering wayfinding assistance, facility information, and personal escorts. Monitors visitor conduct to ensure a safe, welcoming environment, diplomatically stopping and questioning unauthorized individuals as needed. Security & Facility Operations Controls access to all internal facility areas and exterior parking lots. Conducts regular foot patrols across buildings and premises to actively prevent and detect fire, theft, vandalism, and trespassing. Secures, unlocks, and monitors offices and premises according to daily operational schedules. Manages emergency situations and disorderly individuals, coordinating rapidly with local Police and Fire Departments when required. Assists medical staff in safely restraining patients when necessary. Administrative & Team Support Completes accurate, detailed written documentation, including daily activity logs, incident reports, and safety investigations. Remains available to provide additional shift coverage for emergencies and overtime scenarios. Adheres to the operational direction of the department Director and on-duty supervisor. Note: This list is not exhaustive and may be supplemented as necessary. Education & Experience Requirements High School Diploma or GED equivalent (preferred). 2 years of relevant experience (preferred), ideally with a strong background in customer service, hospitality, or guest relations. Credentials & Qualifications SORA license through the State of New Jersey (preferred). Basic Life Support (BLS) certification (preferred).

The Assistant General Manager (AGM) plays a critical leadership role in supporting the daily operations, service delivery, and overall performance of an assigned NYCSBUS depot. Working closely with the General Manager and Maintenance Manager, the AGM helps ensure the safe, reliable, and efficient transportation of students while maintaining compliance with company policies, contractual obligations, and regulatory requirements. The AGM serves as a hands-on operational leader responsible for overseeing frontline transportation staff, including Bus Drivers and Bus Attendants, while ensuring that daily service commitments are met. This role combines field operations management, drivers/attendants and maintenance staff supervision, dispatch coordination, route coverage management, customer service, and administrative responsibilities to support the successful operation of the depot. The position requires a highly visible leadership presence throughout the facility and in the field, with a strong focus on service delivery, operational problem-solving, employee accountability, safety, and customer satisfaction. • Assist the General Manager in the management and execution of all service delivery-related activities within the assigned depot., • Support the daily transportation operation to ensure all routes are properly staffed, dispatched, and serviced., • Monitor operational performance and respond proactively to service disruptions, staffing shortages, route concerns, vehicle issues, and customer complaints., • Serve as the acting operational leader during designated shifts and in the absence of the General Manager., • Operations Data analysis and troubleshoot the results related to departure hub,SVAD and VIA subscription for the AM/PM session, • Directly supervise Bus Drivers and Bus Attendants assigned to the depot., • In collaboration with the CHRCO provide coaching, guidance, and performance feedback to frontline employees., • Promote a culture of safety, accountability, professionalism, and customer service excellence., • Assist in addressing attendance issues, workplace concerns, employee relations matters, and operational performance challenges., • Support employee engagement initiatives and reinforce company expectations regarding conduct, attendance, and performance., • Perform Dispatcher functions as needed to support daily operations., • Coordinate route assignments, route coverage, and staffing adjustments., • Monitor route departures, arrivals, and service performance throughout the day., • Ensure effective communication between drivers, attendants, dispatch, maintenance personnel, and management., • Investigate allegations of drivers/attendants misconduct and respond to employee escalations. To the extent possible and needed include the safety supervisor. All employees' conduct investigations must be reported to the Chief of Human Resources and Compliance Officer in HR., • Perform Road Supervisor duties as required., • Investigate operational incidents, service interruptions, customer concerns, and route performance issues., • Conduct field observations and operational audits to ensure compliance with company standards and safe operating practices., • Conduct End of Day tasks related to collection of trip cards, review for accuracy, conduct walkthrough for depot readiness, inspect the new fleet for cleanliness and damages, report any updates to GM & CSDO., • Respond to emergencies and assist with incident management when necessary., • Assist with workforce scheduling and daily staffing plans., • Support payroll and attendance verification processes as assigned., • Maintain operational records, reports, and documentation., • Analyze operational trends and identify opportunities to improve efficiency, service quality, and employee productivity., • Assist in preparing operational reports and performance metrics for management review., • In collaboration with the Safety and Training Director, facilitate training in the area of incident reporting practices, VIA, problem routes and on time arrivals., • Partner closely with the General Manager, Maintenance Manager, Safety Department, Dispatch Team, Compliance Team, and Human Resources Department to achieve operational objectives., • Support company initiatives, regulatory compliance efforts, and continuous improvement programs., • Participate in depot leadership meetings and contribute to operational planning and decision-making., • The AGM is an active participant of All Hands on Deck and special projects under Service Delivery ie. Parent Capture & Uniform distribution, • Ensure that electric buses assigned to routes are plugged into chargers and are charging., • Report any issues with charging during PM hours to the EV Operations Team., • Use tools developed by technology department to ensure smooth EV Operations The Assistant General Manager is primarily assigned to support the depot's afternoon and closing operations, typically working from approximately 12:00 PM to 9:00 PM . However, operational needs may require flexibility in scheduling. During school openings, peak operational periods, emergency situations, staffing shortages, employee leaves, special projects, or other business-critical circumstances, the AGM may be required to begin work as early as 5:00 AM or work alternative schedules to ensure uninterrupted service delivery. Successful Assistant General Managers demonstrate: • Strong operational leadership and decision-making abilities., • Ability to manage multiple priorities in a fast-paced environment., • Excellent communication and employee management skills., • Strong problem-solving and conflict-resolution capabilities., • Commitment to safety, compliance, and service excellence., • Ability to lead by example while maintaining a high level of accountability and professionalism., • A customer-focused mindset with a dedication to supporting students, families, schools, and employees. The Assistant General Manager serves as a key operational leader within the depot and plays a vital role in ensuring that NYCSBUS consistently delivers safe, reliable, and high-quality transportation services to the students and communities it serves. Pay: $85,000.00 - $110,000.00 per year Benefits: • Paid Time Off, • 401(k) matching, • Dental insurance, • Health insurance, • Vision insurance Schedule: • Evening shift, • Monday to Friday, • Weekends as needed Work Location: In person Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

Job DescriptionBenefits: • 401(k) Job Summary The Program Director is responsible for the overall leadership, administration, and quality management of the agency's New Jersey Division of Developmental Disabilities (DDD) Community-Based Supports (CBS) program. This position oversees program operations, staff performance, regulatory compliance, and service quality to ensure individuals receive person-centered, high-quality supports in accordance with NJ DDD regulations and agency standards. The Program Director collaborates with support coordinators, families, interdisciplinary teams, and agency leadership to promote positive outcomes, maintain compliance, and support organizational growth. Key Responsibilities • Provide leadership and oversight for the daily operations of the DDD Community-Based Supports (CBS) program., • Ensure compliance with New Jersey DDD, Medicaid, HIPAA, and agency policies and procedures., • Supervise, mentor, and evaluate supervisors, Direct Support Professionals (DSPs), and administrative staff., • Lead recruitment, onboarding, training, and staff retention initiatives., • Ensure staffing levels meet participant needs and program requirements., • Review and monitor Individualized Service Plans (ISPs) to ensure services are delivered as authorized., • Collaborate with Support Coordinators, families, guardians, behavioral specialists, nurses, and other members of the interdisciplinary team., • Oversee incident reporting, investigations, corrective actions, and required follow-up in accordance with DDD regulations., • Monitor documentation, progress notes, EVV records, and service delivery to ensure accuracy, completeness, and compliance., • Develop and implement quality assurance and continuous quality improvement initiatives., • Participate in state licensing reviews, accreditation surveys, audits, and regulatory inspections., • Prepare operational reports, performance metrics, and compliance documentation for executive leadership., • Manage departmental budgets, productivity, and resource allocation., • Resolve client, family, and employee concerns in a timely and professional manner., • Develop, implement, and update agency policies, procedures, and best practices., • Foster a positive, person-centered culture that promotes dignity, independence, community inclusion, and high-quality services for individuals receiving supports., • Participate in on-call management and provide operational support during emergencies or critical incidents as needed.

Job Description POSITION SUMMARY: Saint James Health is seeking an experienced Registered Nurse (RN) to serve as the Multisite RN Supervisor, a key leadership role responsible for overseeing vaccine management, clinical staff training, and workflow accountability across multiple locations. This role is critical to driving operational consistency, ensuring regulatory compliance, and elevating the performance of Licensed Practical Nurses (LPNs) and Medical Assistants (MAs). The Multisite RN Supervisor will lead the NJIIS/VFC immunization program with a high level of oversight while developing a skilled, accountable clinical support team across all Saint James Health sites. This is a hands-on leadership position requiring prior supervisory experience, with direct reporting to the Director of Nursing. ESSENTIAL DUTIES AND RESPONSIBILITIES: Immunization Program Oversight • Lead all aspects of vaccine management across multiple sites, including storage, handling, inventory, and documentation., • Ensure full compliance with VFC (Vaccines for Children) /317/ NJIIS, CDC, and New Jersey Department of Health requirements., • Perform monthly audits of vaccine storage, temperature logs, and documentation., • Investigate and resolve vaccine errors; implement corrective action plans., • Maintain audit readiness for HRSA, VFC, and DOH reviews. Clinical Training & Workforce Development • Assist with the implementation of standardized training programs for LPNs and Medical Assistants., • Oversee onboarding, competencies, and annual clinical skills validations (e.g., injections, documentation, workflows)., • Provide ongoing coaching, mentorship, and real-time feedback to clinical staff (LPN's and MA's)., • Identify performance gaps and recommend targeted improvement plans., • Support workforce development initiatives, including certifications and continuing education. Workflow Oversight & Accountability • Monitor and enforce clinical workflows related to immunizations, intake, and patient flow., • Conduct regular audits of LPN and MA workflows, documentation, and task completion., • Ensure adherence to Epic workflows, standing orders, and UDS documentation standards., • Identify inefficiencies and recommend process improvements., • Partner with front desk leadership to ensure appropriate staffing coverage and operational support. Multi-Site Clinical Operations Leadership • Supervise and support clinical support staff (LPNs and MAs) across multiple locations (minimum 20+ staff)., • Travel between sites to ensure consistency in clinical operations and compliance., • Collaborate with DON, Nurse Manager, and leadership to resolve operational challenges., • Lead trainings, and performance improvement initiatives for MA's & LPN's. Quality & Compliance • Support quality initiatives aligned with HRSA UDS measures, including immunization rates and preventive care outcomes., • Ensure adherence to infection control policies and clinical safety standards., • Participate in incident reporting, investigations, and corrective actions, as directed by DON., • Maintain current knowledge of FQHC regulatory requirements and best practices. QUALIFICATIONS: • Active Registered Nurse (RN) license in the State of New Jersey, • Minimum 3–5 years of clinical experience, preferably in an FQHC, ambulatory care or community health, • Minimum 2–3 years of supervisory/management experience, overseeing staff across multiple sites, • Strong experience managing VFC/317/NJIIS immunization programs, including vaccine storage, handling, and compliance; experience in pediatrics, OB/GYN, and family practice preferred, • Experience training and supervising LPNs and Medical Assistants, • Knowledge of FQHC operations, HRSA, UDS, and VFC requirements preferred, • Experience with Epic EMR strongly preferred, • Strong leadership, organizational, and communication skills, • Ability to manage multiple priorities in a fast-paced, mission-driven environment, • Bilingual (English/Spanish)-Preferred Core Competencies • Leadership & Accountability, • Clinical Training & Workforce Development, • Regulatory Compliance & Audit Readiness, • Operational Excellence, • Process Improvement, • Team Collaboration OTHER DUTIES: Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to sit, stand, and walk. The employee must be able to lift and/or move up to 10 pounds.

Job DescriptionPLAZA HEALTHCARE & REHABILITATION CENTERJOB DESCRIPTION – DIRECTOR OF NURSING (DON) Position: Director of Nursing (DON) Department: Nursing Reports To: Administrator Supervises: Assistant Director of Nursing (ADON), Nursing Supervisors, Registered Nurses (RNs), Licensed Practical Nurses (LPNs), Certified Nursing Assistants (CNAs), and other nursing personnel. POSITION SUMMARY The Director of Nursing is responsible for the overall direction, supervision, and management of the Nursing Department. The DON ensures that residents receive high-quality nursing care in accordance with federal and state regulations, facility policies, and established standards of clinical practice. The DON is responsible for maintaining adequate nursing coverage, overseeing clinical operations, developing nursing staff, ensuring regulatory compliance, and promoting resident safety, satisfaction, and quality of care. ESSENTIAL DUTIES AND RESPONSIBILITIES 1. Nursing Department Management Oversee the daily operations of the entire Nursing Department. Provide leadership, direction, and supervision to all nursing personnel. Ensure nursing staff follow facility policies, procedures, and clinical standards. Establish clear expectations and hold nursing personnel accountable for their responsibilities. Conduct regular nursing department meetings and communicate important updates to staff. Work collaboratively with the Administrator and other department heads. 1. Clinical Oversight and Resident Care Ensure residents receive appropriate, timely, and individualized nursing care. Monitor residents' clinical conditions and ensure appropriate interventions are implemented. Oversee assessments, care plans, medication administration, treatments, and documentation. Ensure timely notification of physicians and responsible parties regarding significant changes in condition. Monitor infection prevention and control practices. Oversee clinical incidents, falls, medication errors, pressure injuries, and other adverse events. Ensure appropriate follow-up and corrective actions are implemented when necessary. 1. Staffing and Personnel Management Oversee nursing schedules and ensure adequate staffing levels at all times. Work with the staffing coordinator to address staffing shortages and coverage needs. Participate in interviewing, hiring, training, evaluating, and disciplining nursing personnel. Ensure nursing staff maintain required licenses, certifications, and competencies. Address attendance, performance, and employee conduct issues. Ensure appropriate orientation and ongoing education for nursing staff. 1. Regulatory Compliance and Survey Readiness Ensure compliance with all applicable CMS, New Jersey Department of Health, and other regulatory requirements. Maintain ongoing survey readiness throughout the year. Oversee the development and implementation of Plans of Correction related to nursing deficiencies. Ensure nursing documentation meets regulatory and facility standards. Participate in annual surveys, complaint investigations, and other regulatory visits. Monitor and address nursing-related deficiencies and ensure corrective actions are sustained. 1. Quality Assurance and Performance Improvement (QAPI) Participate in and oversee nursing-related QAPI initiatives. Review clinical indicators, incidents, trends, and quality measures. Identify opportunities for improvement and implement corrective action plans. Monitor the effectiveness of interventions and ensure continued compliance. Work with the interdisciplinary team to improve resident outcomes. 1. Communication and Interdisciplinary Coordination Maintain open communication with the Administrator, Medical Director, attending physicians, and other department heads. Coordinate nursing services with Rehabilitation, Dietary, Social Services, Admissions, and other departments. Address resident and family concerns related to nursing care. Participate in resident care conferences and other facility meetings as needed. 1. Infection Control and Employee Education Ensure proper infection prevention and control practices are followed. Oversee isolation precautions, surveillance, and infection reporting. Ensure staff receive required in-services and ongoing clinical education. Monitor compliance with hand hygiene, PPE use, and other infection control protocols. 1. Additional Responsibilities Ensure nursing policies and procedures are maintained and updated as necessary. Oversee proper utilization and maintenance of nursing equipment and supplies. Ensure emergency preparedness procedures are followed within the Nursing Department. Assist with developing and implementing facility-wide operational initiatives. Perform other duties and responsibilities as assigned by the Administrator. QUALIFICATIONS AND REQUIREMENTS Current, active New Jersey Registered Nurse (RN) license in good standing. Previous nursing leadership experience in a skilled nursing or long-term care facility. Previous DON or ADON experience preferred. Thorough knowledge of CMS regulations, New Jersey Department of Health requirements, and long-term care clinical standards. Strong leadership, communication, organizational, and problem-solving skills. Ability to manage multiple priorities and work effectively in a fast-paced environment. Knowledge of electronic medical records and nursing documentation systems. GENERAL DISCLAIMER This job description is intended to describe the general nature and level of work performed by the Director of Nursing. It is not intended to be an exhaustive list of all duties, responsibilities, or qualifications associated with the position. The employee may be required to perform additional duties and responsibilities as assigned by the Administrator or facility ownership.

Benefits can include Group Health (Medical, Dental, and Vision), Paid Time Off, Paid Holidays, 401(k) matching, Group Life and Disability insurance, Professional Development opportunities, Wellness programs, and a variety of other perks. Working closely with Chief Digital Officers, Chief Data & AI O

LI-DJ1#Keller1 Additional Information Salary Range: $90,000 - $130,000 per year Actual salary will be based on a variety of factors including relevant internal and external experience, knowledge, skills, scope of job, geographical location or other factors permitted by law Benefits: RECON is a Kelle

Sr IT Project Manager Location: Newark, NJ — Hybrid 3 Days Onsite InPerson interview Requirted AutoCAD exp is must 10+ years of extensive experience in leading large, complex projects PMP and/or comparable project management certifications Experience with AutoCAD and CSI-format documents Experienc

The General Manager has proficient knowledge of all operational policies and procedures and of all positions and owns the cost efficiency for the Lounge. As a dynamic and fast-growing company, we offer exciting career opportunities, a diverse and inclusive workplace, and the chance to be part of a t

Proficiency in Microsoft Project, Excel, and Procore. Lead all phases of construction, from planning and estimating through execution and closeout. Develop and maintain project schedules using Microsoft Project.

Oversees and supports the manufacturing and shipping portfolio alongside the Director of Manufacturing. Grants: Applications (DOE, NSF SBIR/STTR, state programs) and post-award management of deliverables, budgets and reporting. Covers handoffs when team members are on leave.

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